Identification of a novel BHD gene

ABSTRACT

The present disclosure relates to Birt-Hogg-Dubé syndrome, nucleic acids encoding the BHD gene, and methods of using the nucleic acids and proteins encoded thereby. In particular, the present disclosure relates to methods of diagnosing BHD disease and related conditions, such as spontaneous pneumothorax and kidney cancer, and methods of treating BHD skin lesions.

CROSS-REFERENCE TO RELATED APPLICATIONS

This is the § 371 U.S. National Stage of International Application No.PCT/US03/17227, filed on May 30, 2003, which was published in Englishunder PCT Article 21(2), and which in turn claims the benefit of U.S.Provisional Application No. 60/385,181, filed May 31, 2002, and U.S.Provisional Application No. 60/390,291, filed Jun. 20, 2002.

FIELD OF THE DISCLOSURE

The present disclosure relates to Birt-Hogg-Dubé syndrome, nucleic acidsencoding the BHD gene, and methods of using the nucleic acids.

BACKGROUND

The triad of dermatologic lesions, including fibrofolliculomas,trichodiscomas and achrocordons, known as the Birt-Hogg-Dubé (BHD)syndrome, was originally described in a Canadian kindred in 1977 (Birtet al., Arch. Dermatol. 113:1674-1677, 1977). Other phenotypic featureswere found to be associated with BHD syndrome including renal neoplasia(Roth et al., J. Amer. Acad. Derm. 29:1055-1056, 1993) and lung cystsand/or spontaneous pneumothorax (Toro et al., Arch Dermatol.135:1195-1202, 1999). When adjusted for age, patients withfibrofolliculomas (benign tumors of the hair follicle) have about aseven-fold increased risk for developing renal neoplasms and a 50-foldincreased risk for developing spontaneous pneumothorax compared withtheir unaffected siblings. Lung cysts develop frequently (83%) inaffected members of BHD families (Zbar et al., Cancer Epidem. Bio. Prev.11:393-400, 2002). Although colon polyps have been reported in BHDpatients (Hornstein et al., Hum. Genet. 33:193-197, 1976; Hornstein etal., Arch. Derm. Res. 253:161-175, 1975), the frequency is notstatistically significant compared to unaffected siblings (Zbar et al.,Cancer Epidem. Bio. Prev. 11:393-400, 2002). Previously, the presentinventors used the original BHD family of Birt, Hogg and Dubé to performa genome-wide scan for linkage and localized the disease gene locus bylinkage analysis in 8 additional families to a 4 cM region of chromosome17p11.2 between D17S1857 and D17S805 (Schmidt et al., Am. J. Hum. Genet.69:876-882, 2001). Linkage to 17p12-q11.2 was also reported in a SwedishBHD pedigree with associated renal neoplasms (Khoo et al., Oncogene 20,5239-5242, 2001). The BHD encoding sequence, however, is unknown.

SUMMARY OF THE DISCLOSURE

Disclosed herein is a BHD encoding sequence and methods of use, severalspecific mutant BHD encoding sequences, and the proteins (folliculins)encoded by these nucleic acid molecules. Also disclosed is a BHDconsensus sequence. Specific embodiments are methods of diagnosing BHDdisease and related conditions. Also provided are methods of treatingBHD skin lesions.

In certain embodiments, the BHD encoding sequence is used in methods forthe differential diagnosis of BHD disease, and in particular examplesthe BHD encoding sequence is used in a diagnostic test for BHD mutationsperformed using a blood sample. This test is particularly useful indetecting asymptomatic mutation carriers in BHD families.

Also disclosed are novel therapies for treatment of BHD skin lesions(fibrofolliculomas). For example, in certain embodiments the methods aremethods of treating BHD skin lesions using a cream containing the BHDprotein, folliculin. Such methods are expected to reduce the size andappearance of the benign hair follicle tumors. Further embodiments aremethods of using the BHD encoding sequence in the differential diagnosisof sporadic kidney cancer. The BHD encoding sequence is the third genefound to be responsible for inherited kidney cancer, and mutationtesting allows for diagnosis and initiation of the proper treatment,which is different for each of the types of kidney cancer caused by thethree genes.

In some embodiments, the methods are methods of using the BHD encodingsequence in the differential diagnosis for spontaneous pneumothorax orcollapsed lung. Collapsed lung can be caused by several factors, and aBHD diagnostic test allows a physician to determine if the emergencysituation resulting from the subject's collapsed lung will recur, andwhether the subject carries the predisposition to develop additionalspontaneous pneumothoraces due to a BHD encoding sequence mutation.

The foregoing and other features and advantages will become moreapparent from the following detailed description of a severalembodiments.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 is a schematic diagram summarizing some specific BHD genemutations

FIG. 2 is a physical map of the BHD critical region on 17p11.2 definedby critical recombinants in Families 243, 210 and 216 showing locationof the BHD gene. FIG. 2A is a map of the BAC tiling path, shown by blackhorizontal lines with arrowheads indicating directional read ofcompleted sequence and GenBank accession numbers. BAC overlaps wereconfirmed by in silico and PCR methods. A single gap was spanned byexons of the COPS3 gene. Locations of polymorphic, markers and geneswere confirmed in silico and by PCR amplification from BAC clones. FIG.2B is a map of the critical recombinants identified in Family 243(D17S2196), Family 210(CA109) and Family 216 (CA138) which define theBHD minimal region to 700 kb. The nonrecombining region is shown inblack shading. FIG. 2C is a map of the location of two overlapping,uncharacterized mRNAs from melanoma (GenBank Accession Nos. BC015725 andBC015687) shown within the 700 kb BHD candidate region. The BHD geneexon/intron structure with 14 coding exons is given.

FIG. 3 is a series of pedigrees showing mutation analysis of the BHDgene and cosegregation with disease in Families 200, 202, and 230. FIG.3A. is a pedigree of Family 200. The pedigree shows cosegregation of theC insertion mutation (C₉) with disease (black symbols, affected status).Individual 9 is an asymptomatic mutation carrier with a history ofspontaneous pneumothorax. Sequence analysis of somatic cell hybrid DNAfrom a BHD patient showed a C insertion in the (C)₈ tract (nt 1733-1740)within exon 11 on the affected chromosome and wild-type (C)₈ tract onthe unaffected chromosome. FIG. 3B. is a pedigree of Family 202. Themutation produced a unique DHPLC heteroduplex peak (insert in blacksymbol) which cosegregated with disease (black symbols, affectedstatus). Unaffected individuals (white symbols, unaffected status) showa wild-type homoduplex DHPLC peak (insert in white symbol). Sequenceanalysis of subcloned PCR product from a BHD affected individual showedthe delAGinsC mutation (nt 1087-1088) in exon 7. FIG. 3C. is a pedigreeof Family 230. The pedigree shows cosegregation of the mutation withdisease (black symbols, affected status). Sequence analysis of exon 12in BHD affected individuals showed a C->G mutation (nt 1844) whichproduces an in-frame terminaton at codon 463.

FIG. 4. shows the results of mutation analysis of the BHD gene andcosegregation with disease in Family 228. Sequence analysis of asubcloned PCR product from a BHD affected individual showed a 28 bpduplication (nt 1378-1405) in exon 9. FIG. 4A. The pedigree showscosegregation of the 28 bp allele with disease (black symbols, affectedstatus). FIG. 4B. PCR products from the exon 9 amplicon wereelectrophoresed on a 4-20% polyacrylamide gradient gel to separate the28 bp duplication allele (341 bp) from the wild-type allele (313 bp).Lane 1, 100 bp MW marker; lanes 2,3,5,7,8 and 9 represent affectedindividuals (black symbols); lanes 4, 6, and 10 represent unaffectedindividuals (white symbols); lane 11, water blank.

FIG. 5A. Northern blot analysis of BHD expression. A 3.8 kb transcriptwas detected in all tissues when a Northern blot (Origene) with 12 majortissues was hybridized with an exon 11 amplicon of the BHD gene. Thesame size band was detected on a minor tissue Northern blot (Origene),which included skin, and a fetal blot (Clontech) containing lung,kidney, liver, and brain. Hybridization of the blots with an exon 4amplicon produced the same 3.8 kb transcript. All lanes were loaded with2 micrograms poly A+RNA. FIG. 5B. Amino acid sequence of the BHDprotein, folliculin, consisting of 579 amino acids. The locations ofmutations identified in BHD patients are double-underlined. Thepredicted motifs in black boxes include: a conserved SLS potentialphosphorylation site (aa 128-130), a glutamic acid-rich coiled-coildomain (aa 283-313), and a N-glycosylation site (aa 494-497). Threemyristoylation sites are triple-underlined (aa 52-57, aa 266-271, aa470-475). Regions of high homology in other species are underlined inblack.

FIG. 6. is a schematic diagram of a putative BHD exon sequence involvedin an alternatively spliced variant (SEQ ID NO: 13). This exon(indicated by the arrow) falls between the first and second exon of thewildtype human BHD cDNA, and the resultant alternative cDNA sequencedoes not include exon 4 of the wildtype sequence.

BRIEF DESCRIPTION OF THE SEQUENCE LISTINGS

The nucleic acid and protein sequences listed in the accompanyingsequence listing is shown using standard letter abbreviations fornucleotide bases, and triple letter code for amino acids, as defined in37 C.F.R. 1.822. Only one strand of each nucleic acid sequence is shown,but the complementary strand is understood as included by any referenceto the displayed strand. In the accompanying sequence listing:

SEQ ID NO: 1 shows the sequence of the human BHD cDNA, along with thesequence of the encoded protein.

SEQ ID NO: 2 shows the sequence the human BHD protein, folliculin.

SEQ ID NO: 3 shows the sequence of the mutant human BHD cDNA containingthe 1087delAGinsC mutation, along with the sequence of the encodedprotein.

SEQ ID NO: 4 shows the sequence of a mutant truncated human folliculin.

SEQ ID NO: 5 shows the sequence of the human BHD cDNA containing the1378→1405dup mutation, along with the sequence of the encoded protein.

SEQ ID NO: 6 shows the sequence of a mutant truncated human folliculin.

SEQ ID NO: 7 shows the sequence of the human BHD cDNA containing the1733insC mutation, along with the sequence of the encoded protein.

SEQ ID NO: 8 shows the sequence of a mutant truncated human folliculin.

SEQ ID NO: 9 shows the sequence of the human BHD cDNA containing the1733delC mutation, along with the sequence of the encoded protein.

SEQ ID NO: 10 shows the sequence of a mutant truncated human folliculin.

SEQ ID NO: 11 shows the sequence of the human BHD cDNA containing theC1844G mutation, along with the sequence of the encoded protein.

SEQ ID NO: 12 shows the sequence of a mutant truncated human folliculin.

SEQ ID NO: 13 shows a putative BHD exon sequence involved in analternatively spliced variant. This exon falls between the first andsecond exon of the wildtype human BHD cDNA, and the resultantalternative cDNA sequence does not include exon 4 of the wildtypesequence.

SEQ ID NO: 14 shows the sequence of the mouse BHD cDNA, along with thesequence of the encoded protein.

SEQ ID NO: 15 shows the sequence of the mouse BHD protein.

SEQ ID NO: 16 shows the sequence of the SKB1 forward primer.

SEQ ID NO: 17 shows the sequence of the SKB2 reverse primer.

SEQ ID NO: 18 shows the sequence of the SKB3 forward primer.

SEQ ID NO: 19 shows the sequence of the SKB4 reverse primer.

SEQ ID NO: 20 shows the sequence of the SKB5 forward primer.

SEQ ID NO: 21 shows the sequence of the SKB6 reverse primer.

SEQ ID NO: 22 shows the sequence of the SKB7 forward primer.

SEQ ID NO: 23 shows the sequence of the SKB8 reverse primer.

SEQ ID NO: 24 shows the sequence of the SKB9 forward primer.

SEQ ID NO: 25 shows the sequence of the SKB10 reverse primer.

SEQ ID NO: 26 shows the sequence of the SKB11 forward primer.

SEQ ID NO: 27 shows the sequence of the SKB12 reverse primer.

SEQ ID NO: 28 shows the sequence of the SKB13 forward primer.

SEQ ID NO: 29 shows the sequence of the SKB14 reverse primer.

SEQ ID NO: 30 shows the sequence of the SKA1 forward primer.

SEQ ID NO: 31 shows the sequence of the SKA2 reverse primer.

SEQ ID NO: 32 shows the sequence of the SKA3 forward primer.

SEQ ID NO: 33 shows the sequence of the SKA4 reverse primer.

SEQ ID NO: 34 shows the sequence of the SKA5 forward primer.

SEQ ID NO: 35 shows the sequence of the SKA6 reverse primer.

SEQ ID NO: 36 shows the sequence of the SKA7 forward primer.

SEQ ID NO: 37 shows the sequence of the SKA8 reverse primer.

SEQ ID NO: 38 shows the sequence of the SKA9 forward primer.

SEQ ID NO: 39 shows the sequence of the SKA10 reverse primer.

SEQ ID NO: 40 shows the sequence of the SKA11 forward primer.

SEQ ID NO: 41 shows the sequence of the SKA12 reverse primer.

SEQ ID NO: 42 shows the sequence of the BHD consensus sequence.

DETAILED DESCRIPTION

I. Abbreviations

BHD: Birt-Hogg-Dubé bp: base pair(s) DNA: deoxyribonucleic acid ELISA:enzyme-linked immunosorbant assay PCR: polymerase chain reactionII: Terms

Unless otherwise noted, technical terms are used according toconventional usage. Definitions of common terms in molecular biology maybe found in Benjamin Lewin, Genes V, published by Oxford UniversityPress, 1994 (ISBN 0-19-854287-9); Kendrew et al. (eds.), TheEncyclopedia of Molecular Biology, published by Blackwell Science Ltd.,1994 (ISBN 0-632-02182-9); and Robert A. Meyers (ed.), Molecular Biologyand Biotechnology: a Comprehensive Desk Reference, published by VCHPublishers, Inc., 1995 (ISBN 1-56081-569-8).

In order to facilitate review of the various embodiments of theinvention, the following explanations of specific terms are provided:

Altered expression: Expression of a biological molecule (for example,mRNA or protein) in a subject or biological sample from a subject thatdeviates from expression if the same biological molecule in a subject orbiological sample from a subject having normal characteristics for thebiological condition associated with the molecule. Normal expression canbe found in a control, a standard for a population, etc. For instance,characteristics of normal expression might include an individual who isnot suffering from BHD syndrome, a population standard of individualsbelieved not to be suffering from BHD syndrome, etc.

Altered expression of a biological molecule may be associated with adisease. The term “associated with” includes an increased risk ofdeveloping the disease as well as the disease itself. For instance,certain altered expression, such as altered BHD nucleic acid or BHDprotein (folliculin) expression, can be described as being associatedwith BHD syndrome.

Altered protein expression, such as altered BHD protein expression,refers to expression of a protein that is in some manner different fromexpression of the protein in a normal (wild type) situation. Thisincludes but is not necessarily limited to: (1) a mutation in theprotein such that one or more of the amino acid residues is different;(2) a short deletion or addition of one or a few amino acid residues tothe sequence of the protein; (3) a longer deletion or addition of aminoacid residues, such that an entire protein domain or sub-domain isremoved or added; (4) expression of an increased amount of the protein,compared to a control or standard amount; (5) expression of an decreasedamount of the protein, compared to a control or standard amount; (6)alteration of the subcellular localization or targeting of the protein;(7) alteration of the temporally regulated expression of the protein(such that the protein is expressed when it normally would not be, oralternatively is not expressed when it normally would be); and (8)alteration of the localized (for example, organ or tissue specific)expression of the protein (such that the protein is not expressed whereit would normally be expressed or is expressed where it normally wouldnot be expressed), each compared to a control or standard.

Controls or standards appropriate for comparison to a sample, for thedetermination of altered expression, include samples believed to expressnormally as well as laboratory values, even though possibly arbitrarilyset, keeping in mind that such values may vary from laboratory tolaboratory. Laboratory standards and values may be set based on a knownor determined population value and may be supplied in the format of agraph or table that permits easy comparison of measured, experimentallydetermined values.

Animal: Living multi-cellular vertebrate organisms, a category thatincludes for example, mammals and birds.

Antisense, Sense, and Antigene: Double-stranded DNA (dsDNA) has twostrands, a 5′−>3′ strand, referred to as the plus strand, and a 3′−>5′strand (the reverse compliment), referred to as the minus strand.Because RNA polymerase adds nucleic acids in a 5′−>3′ direction, theminus strand of the DNA serves as the template for the RNA duringtranscription. Thus, the RNA formed will have a sequence complementaryto the minus strand and identical to the plus strand (except that U issubstituted for T).

Antisense molecules are molecules that are specifically hybridizable orspecifically complementary to either RNA or the plus strand of DNA.Sense molecules are molecules that are specifically hybridizable orspecifically complementary to the minus strand of DNA. Antigenemolecules are either antisense or sense molecules directed to a dsDNAtarget.

Binding or stable binding: An oligonucleotide binds or stably binds to atarget nucleic acid if a sufficient amount of the oligonucleotide formsbase pairs or is hybridized to its target nucleic acid, to permitdetection of that binding. Binding can be detected by either physical orfunctional properties of the target:oligonucleotide complex. Bindingbetween a target and an oligonucleotide can be detected by any procedureknown to one skilled in the art, including both functional and physicalbinding assays. Binding can be detected functionally by determiningwhether binding has an observable effect upon a biosynthetic processsuch as expression of a gene, DNA replication, transcription,translation and the like.

Physical methods of detecting the binding of complementary strands ofDNA or RNA are well known in the art, and include such methods as DNaseI or chemical footprinting, gel shift and affinity cleavage assays,Northern blotting, dot blotting and light absorption detectionprocedures. For example, one method that is widely used, because it isso simple and reliable, involves observing a change in light absorptionof a solution containing an oligonucleotide (or an analog) and a targetnucleic acid at 220 to 300 nm as the temperature is slowly increased. Ifthe oligonucleotide or analog has bound to its target, there is a suddenincrease in absorption at a characteristic temperature as theoligonucleotide (or analog) and the target disassociate from each other,or melt.

The binding between an oligomer and its target nucleic acid isfrequently characterized by the temperature (T_(m)) at which 50% of theoligomer is melted from its target. A higher (T_(m) means a stronger ormore stable complex relative to a complex with a lower (T_(m)).

Biological condition: Designates a condition of a subject that can beassessed through observation or through the analysis of a biologicalsample, for example, expression level of BHD protein.

Biological sample: Any sample in which the presence of a protein and/orongoing expression of a protein may be detected. Suitable biologicalsamples include samples containing genomic DNA or RNA (including mRNA),obtained from body cells of a subject, such as those present inperipheral blood, urine, saliva, tissue biopsy, surgical specimen,amniocentesis samples and autopsy material.

BBD Protein: (see Folliculin).

cDNA (complementary DNA): A piece of DNA lacking internal, non-codingsegments (introns) and transcriptional regulatory sequences. cDNA canalso contain untranslated regions (UTRs) that are responsible fortranslational control in the corresponding RNA molecule. cDNA issynthesized in the laboratory by reverse transcription from messengerRNA extracted from cells.

DNA (deoxyribonucleic acid): A long chain polymer that comprises thegenetic material of most living organisms (some viruses have genescomprising ribonucleic acid (RNA)). The repeating units in DNA polymersare four different nucleotides, each of which comprises one of the fourbases, adenine, guanine, cytosine and thymine bound to a deoxyribosesugar to which a phosphate group is attached. Triplets of nucleotides(referred to as codons) code for each amino acid in a polypeptide. Theterm codon is also used for the corresponding (and complementary)sequences of three nucleotides in the mRNA into which the DNA sequenceis transcribed.

Unless otherwise specified, any reference to a DNA molecule is intendedto include the reverse complement of that DNA molecule. Except wheresingle-strandedness is required by the text herein, DNA molecules,though written to depict only a single strand, encompass both strands ofa double-stranded DNA molecule. Thus, a reference to the nucleic acidmolecule that encodes a specific protein, or a fragment thereof,encompasses both the sense strand and its reverse complement. Thus, forinstance, it is appropriate to generate probes or primers from thereverse complement sequence of the disclosed nucleic acid molecules.

Deletion: The removal of a sequence of DNA, the regions on either sidebeing joined together.

Effective amount of a compound: A quantity of compound sufficient toachieve a desired effect in a subject being treated. An effective amountof a compound can be administered in a single dose, or in several doses,for example daily, during a course of treatment However, the effectiveamount of the compound will be dependent on the compound applied, thesubject being treated, the severity and type of the affliction, and themanner of administration of the compound. The general term“administering to the subject” is understood to include all animals (forexample, humans, apes, dogs, cats, horses, and cows) that have or maydevelop a tumor.

Encode: A polynucleotide is said to “encode” a polypeptide if, in itsnative state or when manipulated by methods well known to those skilledin the art, it can be transcribed and/or translated to produce the mRNAfor and/or the polypeptide or a fragment thereof. The anti-sense strandis the complement of such a nucleic acid, and the encoding sequence canbe deduced therefrom.

Folliculin: A BHD protein that has a coiled-coil domain, threemyristylation sites, and an N-glycosylation site. In some examples,folliculin is the 579 amino acid BHD protein shown in SEQ ID NO: 2.Wild-type human folliculin (SEQ ID NO: 2) shows no homology to any knownproteins. Specific, non-limiting examples of mutant folliculin proteinsare shown in SEQ ID NOs: 4, 6, 8, 10, and 12, and are described in Table2.

Folliculin has been identified in a number of non-human species. Mousefolliculin (SEQ ID NO: 14; MGC37841 gene product, AAH25820 protein) is92% identical to human folliculin (SEQ ID NO: 2). Drosophilamelanogaster folliculin (CG8616 gene product) is 22-36% identical(44-56% positive) to human folliculin. Caenorhabditis elegans folliculin(F22D3.2 gene product, AAK31497 protein) is 27-28% identical (44-52%positive) to human folliculin.

Mutations in the BHD gene, for example mutations that produce truncatedfolliculin proteins, lead to BHD disease. Mutations are particularlylikely to occur in residues 1733-1740 of SEQ ID NO:1, which represent a“hot spot” for expansion or contraction mutations in the BHD encodingsequence.

Functional fragments and variants of a polypeptide: Included are thosefragments and variants that maintain at least one function of the parentpolypeptide. It is recognized that the gene or cDNA encoding apolypeptide can be considerably mutated without materially altering oneor more of the polypeptide's functions. First, the genetic code is wellknown to be degenerate, and thus different codons encode the same aminoacids. Second, even where an amino acid substitution is introduced, themutation can be conservative and have no material impact on theessential functions of a protein (see Stryer, Biochemistry 4^(th) Ed.,(c) W. Freeman & Co., New York, N.Y., 1995). Third, part of apolypeptide chain can be deleted without impairing or eliminating all ofits functions, for example, sequence variants in a protein, such as a 5′or 3′ variant, may retain the full function of an entire protein.Fourth, insertions or additions can be made in the polypeptide chain forexample, adding epitope tags, without impairing or eliminating itsfunctions (Ausubel et al., Current Protocols in Molecular Biology,Greene Publ. Assoc. and Wiley-Intersciences, 1998). Other modificationsthat can be made without materially impairing one or more functions of apolypeptide include, for example, in vivo or in vitro chemical andbiochemical modifications or the incorporation of unusual amino acids.Such modifications include, for example, acetylation, carboxylation,phosphorylation, glycosylation, ubiquination, sumoylation, labeling, forexample, with radionucleides, and various enzymatic modifications, aswill be readily appreciated by those well skilled in the art. A varietyof methods for labeling polypeptides and labels useful for such purposesare well known in the art, and include radioactive isotopes such as ³²P,ligands that bind to or are bound by labeled specific binding partners(for example, antibodies), fluorophores, chemiluminescent agents,enzymes, and antiligands. Functional fragments and variants can be ofvarying length. For example, a fragment may consist of 10 or more, 25 ormore, 50 or more, 75 or more, 100 or more, or 200 or more amino acidresidues.

Heterologous: A type of sequence that is not normally (for example, inthe wild-type sequence) found adjacent to a second sequence. In oneembodiment, the sequence is from a different genetic source, such as avirus or organism, than the second sequence.

Hybridization: Oligonucleotides and their analogs hybridize by hydrogenbonding, which includes Watson-Crick, Hoogsteen or reversed Hoogsteenhydrogen bonding, between complementary bases. Generally, nucleic acidconsists of nitrogenous bases that are either pyrimidines (cytosine (C),uracil (U), and thymine (T)) or purines (adenine (A) and guanine (G)).These nitrogenous bases form hydrogen bonds between a pyrimidine and apurine, and the bonding of the pyrimidine to the purine is referred toas “base pairing.” More specifically, A will hydrogen bond to T or U,and G will bond to C. “Complementary” refers to the base pairing thatoccurs between to distinct nucleic acid sequences or two distinctregions of the same nucleic acid sequence.

In vitro amplification: When used in reference to a nucleic acid,techniques that increase the number of copies of a nucleic acid moleculein a sample or specimen. An example of amplification is the polymerasechain reaction, in which a biological sample collected from a subject iscontacted with a pair of oligonucleotide primers, under conditions thatallow for the hybridization of the primers to nucleic acid template inthe sample. The primers are extended under suitable conditions,dissociated from the template, and then re-annealed, extended, anddissociated to amplify the number of copies of the nucleic acid. Theproduct of in vitro amplification can be characterized byelectrophoresis, restriction endonuclease cleavage patterns,oligonucleotide hybridization or ligation, and/or nucleic acidsequencing, using standard techniques. Other examples of in vitroamplification techniques include strand displacement amplification (seeU.S. Pat. No. 5,744,311); transcription-free isothermal amplification(see U.S. Pat. No. 6,033,881); repair chain reaction amplification (seeWO 90/01069); ligase chain reaction amplification (see EP-A-320 308);gap filling ligase chain reaction amplification (see U.S. Pat. No.5,427,930); coupled ligase detection and PCR (see U.S. Pat. No.6,027,889); and NASBA™ RNA transcription-free amplification (see U.S.Pat. No. 6,025,134).

Isolated: A biological component (such as a nucleic acid molecule,protein or organelle) that has been substantially completely separatedor purified away from other biological components in the cell of theorganism in which the component naturally occurs, for example, otherchromosomal and extra-chromosomal DNA and RNA, proteins and organelles.Nucleic acids and proteins that have been isolated include nucleic acidsand proteins purified by standard purification methods. The term alsoembraces nucleic acids and proteins prepared by recombinant expressionin a host cell as well as chemically synthesized nucleic acids.

Labeled: A biomolecule attached covalently or noncovalently to adetectable label or reporter molecule. Typical labels includeradioactive isotopes, enzyme substrates, co-factors, ligands,chemiluminescent or fluorescent agents, haptens, and enzymes. Methodsfor labeling and guidance in the choice of labels appropriate forvarious purposes are discussed, for example, in Sambrook et al.,Molecular Cloning: A Laboratory Manual, CSHL, New York, 1989 and Ausubelet al., Current Protocols in Molecular Biology, Greene Publ. Assoc. andWiley-Intersciences, 1998. For example, ATP can be labeled in any one ofits three phosphate groups with radioisotopes such as ³²P or ³³P, or inits sugar moiety with a radioisotope such as ³⁵S.

Mammal: This term includes both human and non-human mammals. Similarly,the term subject includes both human and veterinary subjects.

Modulator: An agent that increases or decreases (modulates) the activityof a protein as measured by the change in an experimental parameter. Amodulator can be essentially any compound, such as a chemotherapeuticagent, a polypeptide, a hormone, a nucleic acid, a sugar, a lipid andthe like.

Mutation: Any change of the DNA sequence within a gene or chromosome. Insome instances, a mutation will alter a characteristic or trait(phenotype), but this is not always the case. Types of mutations includebase substitution point mutations (for example, transitions ortransversions), deletions, and insertions. Missense mutations are thosethat introduce a different amino acid into the sequence of the encodedprotein; nonsense mutations are those that introduce a new stop codon.In the case of insertions or deletions, mutations can be in-frame (notchanging the frame of the overall sequence) or frame shift mutations,which may result in the misreading of a large number of codons (andoften leads to abnormal termination of the encoded product due to thepresence of a stop codon in the alternative frame).

This term specifically encompasses variations that arise through somaticmutation, for instance those that are found only in disease cells, butnot constitutionally, in a given individual. Examples of suchsomatically-acquired variations include the point mutations thatfrequently result in altered function of various genes that are involvedin development of cancers. This term also encompasses DNA alterationsthat are present constitutionally, that alter the function of theencoded protein in a readily demonstrable manner, and that can beinherited by the children of an affected individual. In this respect,the term overlaps with “polymorphism,” as defined below, but generallyrefers to the subset of constitutional alterations that have arisenwithin the past few generations in a kindred and that are not widelydisseminated in a population group. In particular embodiments, the termis directed to those constitutional alterations that have major impacton the health of affected individuals.

Nucleotide: This term includes, but is not limited to, a monomer thatincludes a base linked to a sugar, such as a pyrimidine, purine, orsynthetic analogs thereof, or a base linked to an amino acid, as in apeptide nucleic acid (PNA). A nucleotide is one monomer in apolynucleotide. A nucleotide sequence refers to the sequence of bases ina polynucleotide.

Oligonucleotide: A plurality of joined nucleotides joined by nativephosphodiester bonds, between about 6 and about 300 nucleotides inlength. An oligonucleotide analog refers to moieties that functionsimilarly to oligonucleotides but have non-naturally occurring portions.For example, oligonucleotide analogs can contain non-naturally occurringportions, such as altered sugar moieties or inter-sugar linkages, suchas a phosphorothioate oligodeoxynucleotide. Functional analogs ofnaturally occurring polynucleotides can bind to RNA or DNA, and includepeptide nucleic acid (PNA) molecules.

Particular oligonucleotides and oligonucleotide analogs can includelinear sequences up to about 200 nucleotides in length, for example asequence (such as DNA or RNA) that is at least 6 bases, for example atleast 8, 10, 15, 20, 25, 30, 35, 40, 45, 50, 100 or even 200 bases long,or from about 6 to about 50 bases, for example about 10-25 bases, suchas 12, 15 or 20 bases.

Operably linked: A first nucleic acid sequence is operably linked with asecond nucleic acid sequence when the first nucleic acid sequence isplaced in a functional relationship with the second nucleic acidsequence. For instance, a promoter is operably linked to a codingsequence if the promoter affects the transcription or expression of thecoding sequence. Generally, operably linked DNA sequences are contiguousand, where necessary to join two protein-coding regions, in the samereading frame.

Open reading frame: A series of nucleotide triplets (codons) coding foramino acids without any internal termination codons. These sequences areusually translatable into a peptide.

Ortholog: Two nucleic acid or amino acid sequences are orthologs of eachother if they share a common ancestral sequence and diverged when aspecies carrying that ancestral sequence split into two species.Orthologous sequences are also homologous sequences.

Pharmaceutically acceptable carriers: The pharmaceutically acceptablecarriers useful with the compositions provided herein are conventional.Martin, Remington's Pharmaceutical Sciences, published by MackPublishing Co., Easton, Pa., 19th Edition, 1995, describes compositionsand formulations suitable for pharmaceutical delivery of the nucleotidesand proteins herein disclosed.

In general, the nature of the carrier will depend on the particular modeof administration being employed. For instance, parenteral formulationsusually comprise injectable fluids that include pharmaceutically andphysiologically acceptable fluids such as water, physiological saline,balanced salt solutions, aqueous dextrose, glycerol or the like as avehicle. For solid compositions (for example, powder, pill, tablet, orcapsule forms), conventional non-toxic solid carriers can include, forexample, pharmaceutical grades of mannitol, lactose, starch, ormagnesium stearate. In addition to biologically-neutral carriers,pharmaceutical compositions to be administered can contain minor amountsof non-toxic auxiliary substances, such as wetting or emulsifyingagents, preservatives, and pH buffering agents and the like, for examplesodium acetate or sorbitan monolaurate.

Pharmaceutical agent: A chemical compound or composition capable ofinducing a desired therapeutic or prophylactic effect when properlyadministered to a subject or a cell. Incubating includes exposing atarget to an agent for a sufficient period of time for the agent tointeract with a cell. Contacting includes incubating an agent in solidor in liquid form with a cell.

Polypeptide: A polymer in which the monomers are amino acid residuesthat are joined together through amide bonds. When the amino acids arealpha-amino acids, either the L-optical isomer or the D-optical isomercan be used, the L-isomers being preferred. The term polypeptide orprotein as used herein encompasses any amino acid sequence and includesmodified sequences such as glycoproteins. The term polypeptide isspecifically intended to cover naturally occurring proteins, as well asthose that are recombinantly or synthetically produced.

The term polypeptide fragment refers to a portion of a polypeptide thatexhibits at least one useful epitope. The phrase “functional fragmentsof a polypeptide” refers to all fragments of a polypeptide that retainan activity, or a measurable portion of an activity, of the polypeptidefrom which the fragment is derived. Fragments, for example, can vary insize from a polypeptide fragment as small as an epitope capable ofbinding an antibody molecule to a large polypeptide capable ofparticipating in the characteristic induction or programming ofphenotypic changes within a cell. An epitope is a region of apolypeptide capable of binding an immunoglobulin generated in responseto contact with an antigen. Thus, smaller peptides containing thebiological activity of insulin, or conservative variants of the insulin,are thus included as being of use.

The term soluble refers to a form of a polypeptide that is not insertedinto a cell membrane.

Conservative amino acid substitution tables providing functionallysimilar amino acids are well known to one of ordinary skill in the art.The following six groups are examples of amino acids that are consideredto be conservative substitutions for one another:

1) Alanine (A), Serine (S), Threonine (T);

2) Aspartic acid (D), Glutamic acid (E);

3) Asparagine (N), Glutamine (Q);

4) Arginine (R), Lysine (K);

5) Isoleucine (I), Leucine (L), Methionine (M), Valine (V); and

6) Phenylalanine (F), Tyrosine (Y), Tryptophan (W).

Variations in the cDNA sequence that result in amino acid changes,whether conservative or not, are usually minimized in order to preservethe functional and immunologic identity of the encoded protein. Theimmunologic identity of the protein may be assessed by determiningwhether it is recognized by an antibody; a variant that is recognized bysuch an antibody is immunologically conserved. Any cDNA sequence variantwill preferably introduce no more than twenty, and preferably fewer thanten amino acid substitutions into the encoded polypeptide. Variant aminoacid sequences may, for example, be 80%, 90%, or even 95% or 98%identical to the native amino acid sequence. Programs and algorithms fordetermining percentage identity can be found at the NCBI website.

Polymorphism: Variant in a sequence of a gene, usually carried from onegeneration to another in a population. Polymorphisms can be thosevariations (nucleotide sequence differences) that, while having adifferent nucleotide sequence, produce functionally equivalent geneproducts, such as those variations generally found between individuals,different ethnic groups, geographic locations. The term polymorphismalso encompasses variations that produce gene products with alteredfunction, for example, variants in the gene sequence that lead to geneproducts that are not functionally equivalent. This term alsoencompasses variations that produce no gene product, an inactive geneproduct, or decreased or increased activity of the gene product.

Polymorphisms can be referred to, for instance, by the nucleotideposition at which the variation exists, by the change in amino acidsequence caused by the nucleotide variation, or by a change in someother characteristic of the nucleic acid molecule or protein that islinked to the variation (for example, an alteration of a secondarystructure such as a stem-loop, or an alteration of the binding affinityof the nucleic acid for associated molecules, such as polymerases,RNases, and so forth).

Probes and primers: Nucleic acid probes and primers can be readilyprepared based on the nucleic acid molecules provided in thisdisclosure. A probe comprises an isolated nucleic acid attached to adetectable label or reporter molecule. Typical labels includeradioactive isotopes, enzyme substrates, co-factors, ligands,chemiluminescent or fluorescent agents, haptens, and enzymes. Methodsfor labeling and guidance in the choice of labels appropriate forvarious purposes are discussed, for example, in Sambrook et al. (InMolecular Cloning: A Laboratory Manual, CSHL, New York, 1989) andAusubel et al. (In Current Protocols in Molecular Biology, Greene Publ.Assoc. and Wiley-Intersciences, 1992).

Primers are short nucleic acid molecules, preferably DNAoligonucleotides 10 nucleotides or more in length. More preferably,longer DNA oligonucleotides can be about 15, 17, 20, or 23 nucleotidesor more in length. Primers can be annealed to a complementary target DNAstrand by nucleic acid hybridization to form a hybrid between the primerand the target DNA strand, and then the primer extended along the targetDNA strand by a DNA polymerase enzyme. Primer pairs can be used foramplification of a nucleic acid sequence, for example, by the polymerasechain reaction (PCR) or other nucleic-acid amplification methods knownin the art.

Methods for preparing and using probes and primers are described, forexample, in Sambrook et al. (In Molecular Cloning: A Laboratory Manual,CSHL, New York, 1989), Ausubel et al. (In Current Protocols in MolecularBiology, Greene Publ. Assoc. and Wiley-Intersciences, 1998), and Inniset al. (PCR Protocols, A Guide to Methods and Applications, AcademicPress, Inc., San Diego, Calif., 1990). PCR primer pairs can be derivedfrom a known sequence, for example, by using computer programs intendedfor that purpose such as Primer (Version 0.5, ® 1991, WhiteheadInstitute for Biomedical Research, Cambridge, Mass.). One of ordinaryskill in the art will appreciate that the specificity of a particularprobe or primer increases with its length. Thus, for example, a primercomprising 30 consecutive nucleotides of BHD encoding nucleotide willanneal to a target sequence, such as a BHD encoding sequence homologfrom the gene family contained within a human genomic DNA library, witha higher specificity than a corresponding primer of only 15 nucleotides.Thus, in order to obtain greater specificity, probes and primers can beselected that comprise at least 17, 20, 23, 25, 30, 35, 40, 45, 50 ormore consecutive nucleotides of BHD nucleotide sequences.

The disclosure thus includes isolated nucleic acid molecules thatcomprise specified lengths of the disclosed BHD cDNA sequences. Suchmolecules can comprise at least 17, 20, 23, 25, 30, 35, 40, 45, or 50consecutive nucleotides of these sequences, and can be obtained from anyregion of the disclosed sequences. By way of example, the BHD cDNAsequences can be apportioned into halves, thirds or quarters based onsequence length, and the isolated nucleic acid molecules can be derivedfrom the first or second halves of the molecules, from any of the threethirds or any of the four quarters. By way of example, the human BHDcDNA, ORF, coding sequence and gene sequences can be apportioned intoabout halves, thirds or quarters based on sequence length, and theisolated nucleic acid molecules (for example, oligonucleotides) can bederived from the first or second halves of the molecules, from any ofthe three thirds, or any of the four quarters. The cDNA also could bedivided into smaller regions, for example about eighths, sixteenths,twentieths, fiftieths and so forth, with similar effect.

Another mode of division is to select the 5′ (upstream) and/or 3′(downstream) region associated with a BHD encoding sequence, or toselect an intron or portion thereof.

Protein: A biological molecule expressed by a gene and comprised ofamino acids.

Purified: In a more pure form than is found in nature. The term purifieddoes not require absolute purity; rather, it is intended as a relativeterm. Thus, for example, a purified protein preparation is one in whichthe protein referred to is more pure than the protein in its naturalenvironment within a cell.

The term substantially purified as used herein refers to a molecule (forexample, a nucleic acid, polypeptide, oligonucleotide, etc.) that issubstantially free of other proteins, lipids, carbohydrates, or othermaterials with which it is naturally associated. In one embodiment, themolecule is a polypeptide that is at least 50% free of other proteins,lipids, carbohydrates, or other materials with which it is naturallyassociated. In another embodiment, the polypeptide is at least at least80% free of other proteins, lipids, carbohydrates, or other materialswith which it is naturally associated. In yet other embodiments, thepolypeptide is at least 90% or at least 95% free of other proteins,lipids, carbohydrates, or other materials with which it is naturallyassociated.

Recombinant: A nucleic acid that has a sequence that is not naturallyoccurring or has a sequence that is made by an artificial combination oftwo otherwise separated segments of sequence. This artificialcombination can be accomplished by chemical synthesis or, more commonly,by the artificial manipulation of isolated segments of nucleic acids,for example, by genetic engineering techniques.

Sequence identity: The similarity between two nucleic acid sequences, ortwo amino acid sequences, is expressed in terms of the similaritybetween the sequences, otherwise referred to as sequence identity.Sequence identity is frequently measured in terms of percentage identity(or similarity or homology); the higher the percentage, the more similarthe two sequences are. Homologs or orthologs of the BHD protein, and thecorresponding cDNA sequence, will possess a relatively high degree ofsequence identity when aligned using standard methods. This homologywill be more significant when the orthologous proteins or cDNAs arederived from species that are more closely related (for example, humanand chimpanzee sequences), compared to species more distantly related(for example, human and C. elegans sequences).

By way of example, the mouse ortholog (SEQ ID NO: 14; MGC37841 geneproduct, AAH25820 protein) is 92% identical to human folliculin (SEQ IDNO: 2). The Drosophila melanogaster ortholog (CG8616 gene product) is22-36% identical (44-56% positive) to the human folliculin. Finally, theCaenorhabditis elegans ortholog (F22D3.2 gene product, AAK31497 protein)is 27-28% identical (4452% positive) to the human folliculin.

Methods of alignment of sequences for comparison are well known in theart. Various programs and alignment algorithms are described in Smithand Waterman J. Mol. Biol. 147(1): 195-197, 1981; Needleman and WunschJ. Mol. Biol. 48: 443-453, 1970; Pearson and Lipman Proc. Natl. Acad.Sci. USA 85: 2444-2448, 1988; Higgins and Sharp Gene, 73: 237-244, 1988;Higgins and Sharp CABIOS 5: 151-153, 1989; Corpet et al. Nuc. Acids Res.16, 10881-10890, 1988; Huang et al Computer Appls. in the Biosciences 8,155-165, 1992; and Pearson et al. Meth. Mol. Bio. 24, 307-331, 1994.Furthermore, Altschul et al. (J. Mol. Biol. 215:403-410, 1990) present adetailed consideration of sequence alignment methods and homologycalculations.

The NCBI Basic Local Alignment Search Tool (BLAST) (Altschul et al. J.Mol. Biol. 215: 403-410, 1990) is available from several sources,including the National Center for Biotechnology Information (NCBI,Bethesda, Md.) and on the Internet, for use in connection with thesequence analysis programs blastp, blastn, blastx, tblastn and tblastx.The Search Tool can be accessed at the NCBI website, together with adescription of how to determine sequence identity using this program.

An alternative indication that two nucleic acid molecules are closelyrelated is that the two molecules hybridize to each other understringent conditions. Stringent conditions are sequence-dependent andare different under different environmental parameters. Generally,stringent conditions are selected to be about 5° C. to 20° C. lower thanthe thermal melting point (T_(m)) for the specific sequence at a definedionic strength and pH. The T_(m) is the temperature (under defined ionicstrength and pH) at which 50% of the target sequence remains hybridizedto a perfectly matched probe or complementary strand. Conditions fornucleic acid hybridization and calculation of stringencies can be foundin Sambrook et al. (1989) Molecular Cloning: A Laboratory Manual, CSHL,New York and Tijssen (1993) Laboratory Techniques in Biochemistry andMolecular Biology—Hybridization with Nucleic Acid Probes Part I, Chapter2, Elsevier, N.Y. Nucleic acid molecules that hybridize under stringentconditions to a human BHD encoding sequence will typically hybridize toa probe based on either an entire human BHD encoding sequence orselected portions of the gene under wash conditions of 2×SSC at 50° C. Amore detailed discussion of hybridization conditions is presented below.

Nucleic acid sequences that do not show a high degree of identity cannevertheless encode similar amino acid sequences, due to the degeneracyof the genetic code. It is understood that changes in nucleic acidsequence can be made using this degeneracy to produce multiple nucleicacid molecules that all encode substantially the same protein.

Small interfering RNAs: Synthetic or naturally-produced small doublestranded RNAs (dsRNAs) that can induce gene-specific inhibition ofexpression in invertebrate and vertebrate species are provided. TheseRNAs are suitable for interference or inhibition of expression of atarget gene and comprise double stranded RNAs of about 15 to about 40nucleotides containing a 3′ and/or 5′ overhang on each strand having alength of 0- to about 5-nucleotides, wherein the sequence of the doublestranded RNAs is essentially identical to a portion of a coding regionof the target gene for which interference or inhibition of expression isdesired. The double stranded RNAs can be formed from complementaryssRNAs or from a single stranded RNA that forms a hairpin or fromexpression from a DNA vector.

Specific binding agent: An agent that binds substantially only to adefined target. Thus a BHD protein-specific binding agent bindssubstantially only the BHD protein. As used herein, the phrase BHDprotein-specific binding agent includes anti-BHD protein antibodies(such as monoclonal antibodies) and other agents (such as solublereceptors) that bind substantially only to the BHD protein. BHD specificbinding agents can also be produced that bind substantially only tomutant BHD protein and not to wild-type BHD protein, or that bindsubstantially only to wild-type BHD protein and not to mutant BHDprotein. Such specific binding agents are described in greater detailbelow. Such specific binding agents are useful in the detection of BHDdisease.

Anti-BHD protein antibodies can be produced using standard proceduresdescribed in a number of texts, including Harlow and Lane (Antibodies, ALaboratory Manual, CSHL, New York, 1988). The determination that aparticular agent binds substantially only to the BHD protein can readilybe made by using or adapting routine procedures. One suitable in vitroassay makes use of the Western blotting procedure (described in manystandard texts, including Harlow and Lane, Antibodies, A LaboratoryManual, CSHL, New York, 1988). Western blotting can be used to determinethat a given BHD protein (folliculin) binding agent, such as an anti-BHDprotein monoclonal antibody, or folliculin amino- or carboxy-terminalpeptide-derived polyclonal antibody, binds substantially only to the BHDprotein. A phosphospecific binding agent specifically binds to a peptidecontaining a phosphorylated residue.

Shorter fragments of antibodies can also serve as specific bindingagents. For instance, Fabs, Fvs, and single-chain Fvs (SCFvs) that bindto folliculin would be BHD-specific binding agents. These antibodyfragments are defined as follows: (1) Fab, the fragment which contains amonovalent antigen-binding fragment of an antibody molecule produced bydigestion of whole antibody with the enzyme papain to yield an intactlight chain and a portion of one heavy chain; (2) Fab′, the fragment ofan antibody molecule obtained by treating whole antibody with pepsin,followed by reduction, to yield an intact light chain and a portion ofthe heavy chain; two Fab′ fragments are obtained per antibody molecule;(3) (Fab′)2, the fragment of the antibody obtained by treating wholeantibody with the enzyme pepsin without subsequent reduction; (4)F(ab′)2, a dimer of two Fab′ fragments held together by two disulfidebonds; (5) Fv, a genetically engineered fragment containing the variableregion of the light chain and the variable region of the heavy chainexpressed as two chains; and (6) single chain antibody (SCA), agenetically engineered molecule containing the variable region of thelight chain, the variable region of the heavy chain, linked by asuitable polypeptide linker as a genetically fused single chainmolecule. Methods of making these fragments are routine.

Specifically hybridizable and specifically complementary are terms thatindicate a sufficient degree of complementarity such that stable andspecific binding occurs between the oligonucleotide (or its analog) andthe DNA or RNA target. The oligonucleotide or oligonucleotide analogneed not be 100% complementary to its target sequence to be specificallyhybridizable. An oligonucleotide or analog is specifically hybridizablewhen binding of the oligonucleotide or analog to the target DNA or RNAmolecule interferes with the normal function of the target DNA or RNA,and there is a sufficient degree of complementarity to avoidnon-specific binding of the oligonucleotide or analog to non-targetsequences under conditions where specific binding is desired, forexample under physiological conditions in the case of in vivo assays orsystems. Such binding is referred to as specific hybridization.

Hybridization conditions resulting in particular degrees of stringencywill vary depending upon the nature of the hybridization method ofchoice and the composition and length of the hybridizing nucleic acidsequences. Generally, the temperature of hybridization and the ionicstrength (especially the Na⁺ concentration) of the hybridization bufferwill determine the stringency of hybridization, though waste times alsoinfluence stringency. Calculations regarding hybridization conditionsrequired for attaining particular degrees of stringency are discussed bySambrook et al. (ed.), Molecular Cloning: A Laboratory Manual, 2nd ed.,vol. 1-3, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.,1989, chapters 9 and 11, herein incorporated by reference.

The following is an exemplary set of hybridization conditions:

Very High Stringency (detects sequences that share 90% identity)Hybridization: 5x SSC at 65° C. for 16 hours Wash twice: 2x SSC at roomtemperature (RT) for 15 minutes each Wash twice: 0.5x SSC at 65° C. for20 minutes each

High Stringency (detects sequences that share 80% identity or greater)Hybridization: 5x-6x SSC at 65° C.-70° C. for 16-20 hours Wash twice: 2xSSC at RT for 5-20 minutes each Wash twice: 1x SSC at 55° C.-70° C. for30 minutes each

Low Stringency (detects sequences that share greater than 50% identity)Hybridization: 6x SSC at RT to 55° C. for 16-20 hours Wash at leasttwice: 2x-3x SSC at RT to 55° C. for 20-30 minutes each.

Subject: Living multi-cellular vertebrate organisms, a category thatincludes both human and non-human mammals.

Target sequence: “Target sequence” is a portion of ssDNA, dsDNA, or RNAthat, upon hybridization to a therapeutically effective oligonucleotideor oligonucleotide analog, results in the inhibition of expression. Forexample, hybridization of therapeutically effectively oligonucleotide toa BHD target sequence results in inhibition of BHD expression. Either anantisense or a sense molecule can be used to target a portion of dsDNA,as both will interfere with the expression of that portion of the dsDNA.The antisense molecule can bind to the plus strand, and the sensemolecule can bind to the minus strand. Thus, target sequences can bessDNA, dsDNA, and RNA.

Test compound: A test compound can be essentially any compound, such asa chemotherapeutic, a polypeptide, a hormone, a nucleic acid, a sugar, alipid and the like.

Therapeutically effective amount of a folliculin protein: A quantity offolliculin protein sufficient to achieve a desired effect in a subjectbeing treated. For instance, this can be the amount necessary to inhibitor to measurably reduce a skin lesion associated with BHD syndrome.

An effective amount of a folliculin protein may be administered in asingle dose, or in several doses, for example daily or more often,during a course of treatment. However, the effective amount offolliculin or a fragment thereof will be dependent on the folliculinprotein applied, the subject being treated, the severity and type of theaffliction, and the manner of administration of the fusion protein.

The fusion proteins disclosed in the present invention have equalapplication in medical and veterinary settings. Therefore, the generalterm “subject being treated” is understood to include all animals (forexample humans, apes, dogs, cats, horses, and cows) that are or maydisplay a symptom of BHD syndrome that is susceptible to folliculinprotein-mediated amelioration.

Transfected: A process by which a nucleic acid molecule is introducedinto cell, for instance by molecular biology techniques, resulting in atransfected cell. As used herein, the term transfection encompasses alltechniques by which a nucleic acid molecule might be introduced intosuch a cell, including transduction with viral vectors, transfectionwith plasmid vectors, and introduction of DNA by electroporation,lipofection, and particle gun acceleration.

Treating a disease: Includes inhibiting or preventing the partial orfull development or progression of a disease, for example in a personwho is known to have a predisposition to a disease. Furthermore,treating a disease refers to a therapeutic intervention that amelioratesat least one sign or symptom of a disease or pathological condition, orinterferes with a pathophysiological process, after the disease orpathological condition has begun to develop.

Vector: A nucleic acid molecule as introduced into a host cell, therebyproducing a transfected host cell. Recombinant DNA vectors are vectorshaving recombinant DNA. A vector can include nucleic acid sequences thatpermit it to replicate in a host cell, such as an origin of replication.A vector can also include one or more selectable marker genes and othergenetic elements known in the art. Viral vectors are recombinant DNAvectors having at least some nucleic acid sequences derived from one ormore viruses.

Unless otherwise explained, all technical and scientific terms usedherein have the same meaning as commonly understood by one of ordinaryskill in the art to which this invention belongs. The singular terms“a,” “an,” and “the” include plural referents unless context clearlyindicates otherwise. Similarly, the word “or” is intended to include“and” unless the context clearly indicates otherwise. “Comprises” means“includes.” Hence “comprising A or B” means include A, or B, or A and B.It is further to be understood that all base sizes or amino acid sizes,and all molecular weight or molecular mass values, given for nucleicacids or polypeptides are approximate, and are provided for description.Although methods and materials similar or equivalent to those describedherein can be used in the practice or testing of the present invention,suitable methods and materials are described below. All publications,patent applications, patents, and other references mentioned herein areincorporated by reference in their entirety. In case of conflict, thepresent specification, including explanations of terms, will control. Inaddition, the materials, methods, and examples are illustrative only andnot intended to be limiting.

III. Identification of a BHD Encoding Sequence

This disclosure provides BHD encoding sequences and proteins. These wereidentified by recombination mapping, which showed a disease-segregatinginsertion/deletion mutation within a previously uncharacterized gene.The full-length BHD cDNA sequence (SEQ ID NO: 1) was then isolated andsequenced from multiple cDNA libraries, and the predicted proteinproduct (SEQ ID NO: 2) was based on computer-generated predictions.Methods of using these BHD encoding sequences and proteins are alsoprovided herein.

Recombination mapping was used to narrow the minimal BHD region to 700kb. Known candidate genes and uncharacterized mRNAs from within this 700kb region were then screened for mutations in a panel of subjects whohad been diagnosed with BHD. In five of nine BHD kindreds, adisease-cosegregating insertion/deletion mutation was identified in amononucleotide (C)₈ tract within a previously uncharacterized gene(residues 1733-1740 of SEQ ID NO:1). This mutation produced a frameshiftpredicting a premature termination of the protein translation. Anadditional 22 of 53 BHD family probands were tested that were found toharbor the mononucleotide C tract insertion/deletion mutation,indicating that this sequence (residues 1733-1740 of SEQ ID NO:1) is a“hot spot” for expansion or contraction mutations in the BHD encodingsequence. Thus, other mutations are likely to be found in this region,in particular. In addition, several other germline BHD encoding sequencemutations were identified in the patient panel that resulted inframeshifts and predicted protein truncations. All of the mutationscosegregated with disease in BHD families, and none were present in 160normal individuals tested for the mutations.

The full-length BHD cDNA sequence (SEQ ID NO: 1) was then isolated andsequenced from multiple cDNA libraries. Northern blot analysis revealeda 3.8 kb transcript expressed in most normal fetal and adult tissues,including lung, kidney and skin. The predicted 579 amino acid BHDprotein (SEQ ID NO: 2), also referred to herein as folliculin, has acoiled-coil domain, three myristylation sites, and an N-glycosylationsite, based on computer program-generated predictions. The proteinsequence shows no homology to any known proteins. The identified mutantBHD mRNA sequences and encoded mutant folliculin proteins are shown inSEQ ID NOs: 3-12, and are described more fully below and in Table 2. ABHD consensus sequence is shown in SEQ ID NO: 42. One embodiment of thedisclosure is a cell, for example a human cell, that has beentransformed with a BHD nucleic acid sequence.

The discovery of germline BHD encoding sequence mutations responsiblefor the BHD syndrome makes possible the understanding of the biologicalrole of the BHD protein, folliculin, in pathways common to skin, lungand kidney organogenesis, and to new treatments for BHD skin lesions andmore effective therapies for renal cancer. In particular, mutations inthe gene can be used in the differential diagnosis of BHD disease and ina DNA diagnostic test for BHD mutations, for instance using a bloodsample. Such tests are particularly useful in detecting asymptomaticmutation carriers in BHD families.

Identification of the BHD encoding sequence also makes possible noveltherapies for treatment of BHD skin lesions (fibrofolliculomas). Forexample, creams or other preparations containing the BID protein,folliculin, are proposed for use to reduce the size and appearance ofthe benign hair follicle tumors. Furthermore, the BHD encoding sequenceis used in the differential diagnosis of sporadic kidney cancer; the BHDencoding sequence is the third gene found to be responsible forinherited kidney cancer, and mutation testing allows diagnosis andinitiation of the proper treatment, which is different for each of thetypes of kidney cancer caused by the three genes.

Additionally, the BHD encoding sequence is used in the differentialdiagnosis for spontaneous pneumothorax or collapsed lung, as well as indiagnosing a propensity to develop spontaneous pneumothorax. Collapsedlung can be caused by several factors, and a BHD diagnostic test allowsa physician to determine if the emergency situation resulting from thesubject's collapsed lung is likely to recur, and whether the subjectcarries the predisposition to develop additional spontaneouspneumothoraces due to a BHD encoding sequence mutation. Furthermore, theBHD encoding sequence is used in the differential diagnosis for renalneoplasms and fibrofolliculomas, as well as in diagnosing a propensityto develop renal neoplasms and fibrofolliculomas.

Other embodiments are isolated nucleic acid sequences that hybridizewith BHD nucleic acid sequence under low stringency, high stringency, orvery high stringency conditions. A further embodiment is apharmaceutical composition that includes a folliculin protein and apharmaceutically acceptable carrier or diluent. The pharmaceuticalcomposition is used, for example, in treating BHD disease.

Still other embodiments are single-stranded oligonucleotides thathybridize under highly stringent conditions to a nucleic acid moleculehaving the sequence of a mutant BHD sequence that encodes a truncatedBHD protein associated with BHD disease, but that does not hybridizeunder highly stringent conditions to SEQ ID NO: 1. For example, incertain embodiments, the oligonucleotide hybridizes under highlystringent conditions to the mutant BHD sequence shown in SEQ ID NOs: 4,6, 8, 10, or 12. In some embodiments, the oligonucleotide includes atleast 10 consecutive nucleotides of the complements of SEQ ID NOs: 4, 6,8, 10, or 12. In yet still another embodiment, the oligonucleotide isincluded in an array of nucleic acid molecules attached to a solidsupport. In particular embodiments, the oligonucleotide recognizes oneor more of the following mutations: a) deletion of the guanosine ofposition 1088 of SEQ ID NO: 1, b) insertion of the nucleic acid sequenceGTGTTGCCAGAGAGTACAGAAAGCCCCT at position 1389 of SEQ ID NO: 1, c)insertion of a cytosine at position 1741 of SEQ ID NO: 1, d) deletion ofthe cytosine at position 1740 of SEQ ID NO: 1, or e) substitution of acytosine for the guanine at position 1844 of SEQ ID NO: 1.

Yet still another embodiment is an antisense oligonucleotide thatinhibits the expression of the BHD protein encoded by SEQ ID NO. 1.Further embodiments are methods that include obtaining a sample ofnucleic acid from a subject, and determining an identity of a nucleotidethat results in truncation of the BHD protein. In certain examples, thedetermining step includes amplifying at least a portion of a nucleicacid molecule comprising the BHD gene. In certain other examples thedetermining step includes sequencing at least a portion of a nucleicacid molecule comprising the BHD gene. In still other examples, themethod includes determining a propensity to develop a conditionassociated with BHD disease, and in particular examples, the conditionincludes fibrofolliculoma, renal neoplasia, or spontaneous pneumothorax.

Other embodiments include a purified polypeptide having an amino acidsequence that includes the sequence as set forth in SEQ ID NO: 2 orsequences having at least 95% sequence identity to SEQ ID NO: 2. Incertain examples, sequence has at least 98% sequence identity to SEQ IDNO: 2. Also disclosed is a nucleic acid that encodes the polypeptide ofclaim 53. In particular examples, the purified polypeptide of claim 53includes SEQ ID NO: 2 with 0 to 10 conservative amino acidsubstitutions.

Still other embodiments are purified polypeptides that bind specificallyto an antibody that binds specifically to BHD protein. Some examplesinclude a purified antibody that selectively binds to an epitope of aBHD protein. In some examples, the epitope is a region on the BHDprotein that is truncated in BHD disease. In particular examples, theepitope is within amino acid residues 479 to 579 of SEQ ID NO: 2, and incertain examples the antibody binds specifically to a mutant form of BHDbut not to a normal form of BHD.

EXAMPLES Example 1 Identification and Characterization of the BHD Gene

The triad of dermatologic lesions, including fibrofolliculomas,trichodiscomas and achrocordons, known as the Birt-Hogg-Dubé syndrome(BHD), was originally described in a Canadian kindred in 1977 (Birt etal., Arch. Dermatol. 113:1674-1677, 1977). Other phenotypic featureswere found to be associated with BHD including renal neoplasia (Roth etal., J. Amer. Acad. Derm. 29:1055-1056, 1993; Toro et al., Arch.Dermatol. 135:1195-1202, 1999), lung cysts and/or spontaneouspneumothorax (Toro et al., Arch. Dermatol. 135:1195-1202, 1999; Binet etal., Ann. Dermatol. Venereol. 113:928-930, 1986). When adjusted for age,patients with fibrofolliculomas have a 7-fold increased risk fordeveloping renal neoplasms and a 50-fold increased risk for developingspontaneous pneumothorax compared with their unaffected siblings (Zbaret al., Cancer Epidem. Bio. Prev. 11:393-400, 2002). Lung cysts developfrequently (83%) in affected members of BHD families (Roth et al., J.Amer. Acad. Derm. 29:1055-1056, 1993; Toro et al., Arch. Dermatol.135:1195-1202, 1999; Zbar et al., Cancer Epidem. Bio. Prev. 11:393-400,2002). Renal tumors associated with BHD include chromophobe (thepredominant histologic variant), oncocytoma, oncocytic hybrid (a newlydescribed hybrid between chromophobe and oncocytoma; Tickoo et al.,Amer. J. Surg. Pathol. 23:1094-1101, 1999) and clear cell (Zbar et al.,Cancer Epidem. Bio. Prev. 11:393-400, 2002). The BHD disease locus wasinitially localized by linkage analysis in nine families to a 4 cMregion of chromosome 17p11.2 between D17S1857 and D17S805 (Schmidt etal., Am. J. Hum. Genet. 69:876-882, 2001). Linkage to a 35 cMoverlapping region spanning 17p12-q11.2 was reported in a Swedish BHDpedigree with associated renal neoplasms (Khoo et al., Oncogene20:5239-5242, 2001).

Methods

Patient Recruitment and Sampling

Families affected with BHD were recruited and evaluated at the ClinicalCenter, National Institutes of Health, and also on field trips. Patientswere interviewed for a prior history of renal tumors and spontaneouspneumothorax, and were evaluated by a dermatologist. Affected status wasconfirmed by the presence of 10-100 skin papules on the face, neck orupper torso with at least one histologically proven fibrofolliculoma.Blood samples were drawn for DNA preparation and to establishEBV-immortalized B cell lines.

Development of Microsatellites

To increase the density of microsatellite markers in the region of BHDlinkage, we identified new polymorphic di-, tri- and tetranucleotidetracts by BLAST of (CA)₁₆, (TATG)₈ and (TGC)₈ against the BAC genomicsequences from the region. Primers were designed to amplify potentialpolymorphic microsatellites and selected for a heterozygosity >0.6 in apanel of 8 unrelated individuals. Microsatellite genotyping andhaplotype analysis was performed as described (Schmidt et al., Am. J.Hum. Genet. 69:876-882, 2001).

Candidate Gene Selection and Analysis

The BHD critical region at 17p11.2 was examined for known genes,uncharacterized mRNAs, spliced EST clusters, unspliced EST clusters, andpredicted gene exons (in that order). These categories are clearlydelineated by the University of California, Santa Cruz (UCSC) humangenome browser, which served as a primary reference. Additional detailswere obtained from Celera, NCBI, and EnsembI human and mouse genomeassemblies, and annotation of individual BAC clones by Doubletwist.

Exon/intron boundaries were determined by BLAST alignment of the cDNA ofeach candidate gene with BAC genome sequence. Primers located inneighboring introns at least 20 base pairs from the splice junctionswere designed with the aid of Oligo Tech ver. 1 (Oligos Etc & OligoTherapeutics). For large exons, overlapping amplicons were generatedwhich covered the entire coding sequence.

Candidate gene exons were amplified from a panel of patientsrepresenting nine families affected with BHD and 3 unaffectedindividuals to detect nondisease-related mutations. Standard PCRconditions were employed with Amplitaq (Perlin Elmer) or Taq polymerases(Invitrogen). PCR products were quantitated by agarose gelelectrophoresis and purified using Multiscreen PCR cleanup plates(Millipore). Double-stranded sequencing reactions (10 μl) using Big DyeTerminators ready reaction mix (Applied Biosystems) were purified usingPerforma plates (Edge Biosystems) and electrophoresed on an ABI 3700genetic analyzer.

Chromatograms were aligned and analyzed using Lasergene (DNAStar).Alignments were examined using the conflict finder to locatePhred-identified discrepancies, then forward and reverse chromatogramsfrom each affected patient were manually examined to locate additionalsecondary peaks. Sequence variants found in one or more affectedpatients (but not in unaffected individuals) were examined forcosegregation with disease in their respective families by denaturinghigh performance liquid chromatography (DHPLC) or single-strandedsequencing. Insertions and deletions were subcloned with a Topo CloningKit (Invitrogen) and sequenced. A minimum of 160 normal individuals wereexamined for the presence of each disease-associated sequence variant.DHPLC was performed using a Transgenomic WAVE® system with a DNASep®column. Temperature predictions were obtained by the Stanford meltalgorithm or Wavemaker (Transgenomic). Runs were nine minutes andincluded a 75% acetonitrile wash followed by a high A buffer rinse (toclear acetonitrile).

Analysis of the BHD Gene

Two overlapping, uncharacterized, full-length transcripts were sequencedby the NIH Mammalian Gene Collection project and deposited in Genbank onOct. 9 and 11, 2001. The mRNAs (GenBank Accession nos. BC015725 andBC015687) were derived from skin melanoma and were included in the UCSCGenome Browser release of Dec. 22, 2001. These transcripts highlighted aspliced EST cluster located in BAC clone RP11-45M22 (GenBank Accessionno. AC055811), which were analyzed for mutations. Intronic primers weredesigned to amplify 14 coding exons and splice junctions for sequencing.PCR reaction components were standard. Cycling conditions: 95° C. for 3minutes, 94° C. for 45 seconds, annealing T_(m) for 1 minutes, 72° C.for 1 minute for 40 cycles. Primer sequences are shown in Table 1.

Cosegregation of mononucleotide insertion/deletion mutations withaffected haplotype carriers in BHD was determined by single-strandedsequencing of exon 11 amplicons from patient DNA. A 28 bp duplicationallele associated with BHD in Family 228 was separated from thewild-type allele by electrophoresis on a 4-20% gradient polyacrylamidegel (Novex) according to manufacturer's protocols. Family consegregationstudies of missense mutations were conducted using DHPLC.

Northern Blot Analysis

Expression of the BHD gene transcript was evaluated with human polyA+RNA blots (Origene Technologies, Inc.) containing 12 major tissues,including lung and kidney, and 6 minor tissues, including skin. A humanfetal poly A+RNA blot containing kidney, lung, brain, and liver waspurchased from Clontech. The exon 11 amplicon of the BHD gene was usedas a template for RNA antisense probe labeling using Strip-EZ ProbeSynthesis and Removal Kit (Ambion, Inc.) in a linear PCR reaction with³²P-dATP and the antisense gene specific primer according to themanufacturer's protocols. Hybridizations were carried out in Ultrahybsolution with a one hour prehybridization (Ambion, Inc.) at 42° C.overnight, and washed by standard methods.

TABLE 1 Amplicon Annealing Exon Forward Primer Reverse Primer size (bp)temp (C.)  1 SEQ SKB1: SEQ SKB2: 385 64 ID GGACTCTGGCCCTA IDGTACGGCTCAGGGAG NO: 16 AACCC NO: 17 TCAC  2 SEQ SKB3: SEQ SKB4: 225 64ID GACAGCAAGCCTGG ID CATGCTACGAAGGCC NO: 18 GCCAAG NO: 19 TCTAATC  3 SEQSKB5: SEQ SKB6: 256 64 ID AAGGACGATGTGCA ID CACTGCCAGCCCAGC NO: 20TGGTGG NO: 21 TAAG  4 SEQ SKB7: SEQ SKB8: 406 64 ID CACTGCTCTCAGGT IDGGAGGTTTCATGGAG NO: 22 CCTCC NO: 23 TCAATAGG  5 SEQ SKB9: SEQ SKB10: 31064 ID AGTGCCTGCCTCCC ID ACCTAAGAGAGTTTG NO: 24 TGTGC NO: 25 TCGCCCTG  6SEQ SKB11: SEQ SKB12: 354 64 ID TCAGCACAGAGCGG ID GAAGAGGCTTTGATT NO: 26CTCATG NO: 27 TGGTGTCAC  7 SEQ SKB13: SEQ SKB14: 278 64 IDCCAATGTATCGTGA ID GGTCCGAGCTGCTGG NO: 28 CTGCTCTATC NO: 29 CAG  8 SEQSKA1: SEQ SKA2: 607 64 ID GCCCCAGATCAGGA ID CTGGGTGAGCGTCAG NO: 30 ACCTGNO: 31 GTTTGC  9 SEQ SKA3: SEQ SKA4: 313 62 ID CCATGACTGGCTCT IDGTATCTTGGGCTGAA NO: 32 CCTCCT NO: 33 GTCACAGG 10 SEQ SKA5: SEQ SKA6: 29064 ID GCACCAGGCCAATA ID GTCTTTCTCCTGAGCC NO: 34 CTGC NO: 35 CTGTC 11 SEQSKA7: SEQ SKA8: 270 64 ID 5′GGTTCCACTTTGG ID 5′GGTAGTAGAGCATG NO: 36GCCTGAG NO: 37 GATGGCC 12 + 13 SEQ SKA9: SEQ SKA10: 463 64 IDCAGCTCCAGGTTTT ID CACGGTGGGCTAGCG NO: 38 CTCCAGG NO: 39 CAG 14 SEQSKA11: SEQ SKA12: 639 64 ID CCTCGGGAGCAGAC ID ACCAGGGCTCGAGGG NO: 40ATGTTATTG NO: 41 ATTGSomatic Cell Hybrids

Lymphoblasts from several BHD patients (2×10⁷) were fused with mouse RAGcells (2×10⁶) (HPRT-deficient mouse cell line from ATCC). Hybrids wereselected in hypoxanthine aminopterin thymidine (HAT) medium at 37° C.DNA was prepared from expanded colonies and genotyped to determinewhether one copy or both copies of human chromosome 17 were present inthe hybrids.

Full Length Clones and Sequencing

cDNA was obtained from normal adult kidney, and adult and fetal lung(purchased from Clontech). Gene-specific primers were designedapproximately 50 bases from the 5′ and 3′ ends and were used to amplifya 3.2 kb transcript from each library and shotgun sequenced. Takara longand accurate (LA) reagents were used to amplify the transcript withrecommended buffer conditions and extension times. Sequencing primerswere spaced approximately 500 bp apart on both strands for overlapping,double-stranded sequencing. A minimum of 4-fold coverage was obtainedfor each transcript. PCR from these cDNA pools was repeated withAdvantage Polymerase Mix (purchased from Clontech). The structure of thenormal transcript was assembled from the consensus sequence of theseextension reactions.

Several cDNA libraries were screened and a longest clone was isolatedfrom lung. The clone was also shotgun sequenced to >4 fold,double-stranded coverage. Evidence of alternative splicing is currentlyunder investigation for a possible role in disease or normal folliculinfunction. Spliced I.M.A.G.E. clones identified from the UCSC GenomeBrowser were purchased and examined for additional 5′ end sequence.These extended the Clontech transcript sequence 106 bases. 5′ and 3′RACE studies of Clontech cDNA from lung and kidney confirmed thecomplete sequence of the normal gene.

Results

A comprehensive BAC tiling path map was produced by in silico methodsusing BLAST (Altschul et al., J. Mol. Biol. 215:403-410, 1990), andcomparative analysis of genome assemblies, and identified locations ofall known genes, uncharacterized mRNAs and spliced EST clusters in the17p11.2 critical region (FIG. 2A). A PCR-based approach was used toconfirm the locations of genes and markers on overlapping BACs. Theseresults and fluorescence in situ hybridization data provided additionalsupport for the BAC order. This BAC map is in agreement with thephysical map of Lucas et al. (Eur. J. Hum. Genet. 9:892-902, 2001), butconflicts with the current UCSC Genome Browser (December, 2002), Celeraand NCBI (April, 2002) genome assemblies. Difficulties with assembly ofthe 17p11.2 region are most likely due to the presence of low-copynumber repeats [Smith-Magenis Syndrome (SMS) repeats], which cause DNArearrangements, leading to microduplication/deletion syndromes such asSmith-Magenis Syndrome (Chen et al., Ment. Retard. Dev. Disabil Res.Rev. 2:122-129, 1996).

Candidate genes from the critical region were identified based on ESTevidence of expression in skin, lung, and kidney. Exon/intron structurewas determined and intronic primers were designed to amplify all codingsequences and splice junctions. High throughput mutation analysis wasperformed on a panel of patient DNA samples, representing nine BHDfamilies. In total, 321 coding amplicons were sequenced, representing 39known genes, uncharacterized mRNAs, and spliced EST clusters from the 4cM region of linkage on 17p11.2.

In parallel with sequencing, 13 new polymorphic microsatellite markerswere developed to look for new recombinants in the region of linkage.Further analysis of BHD Family 210, described previously (Schmidt etal., Am. J. Hum. Genet 69:876-882, 2001), identified a recombination inthe new distal marker CA109. Additional BHD families were analyzed and aproximal recombination identified in BHD Family 216 in the new markerCA138, which localized the BHD gene to a 1.3 Mb region between CA109 andCA138 (FIG. 2B). Subsequently, a proximal recombination was identifiedin another new BHD family, Family 243, at D17S2196, which narrowed theBHD critical region further to 700 kb (FIG. 2B).

Gene mining within the 700 kb critical region using the December, 2001release of the UCSC Human Genome Browser identified two overlapping,uncharacterized, full-length transcripts from skin melanoma (GenBankAccession nos. BC015725 and BC015687), supported by additional ESTs(FIG. 2C). Northern blot analysis, using probes designed from eithermRNA, revealed a 3.8 kb transcript in most adult and fetal tissues,indicating that these two mRNAs code for a single protein that is widelyexpressed (FIG. 5A).

Sequence analysis of the 14 coding exons contained in these two mRNAsrevealed mutations in 8 of 9 families on the panel (Table 2). A cytosineinsertion mutation in a mononucleotide (C)₈ tract (nt 1733-1740) in exon11 was identified in four BHD families (families 174, 200, 210, 216) andresulted in a frameshift (SEQ ID NO: 7) predicted to truncate theprotein 26 missense amino acids downstream from the mutation (SEQ ID NO:8). A cytosine deletion mutation in the same mononucleotide (C)₈ tract(SEQ ID NO: 9) was identified in one family (Family 201), which wouldtruncate the protein 38 missense amino acids downstream from themutation (SEQ ID NO: 10). Sequence analysis of somatic cell hybridsestablished from patients from several of these BHD families confirmedthe presence of the (C)₉ allele on the affected chromosome 17 and the(C)₈ allele on the wild type chromosome 17 (FIG. 3A). Cosegregation ofthese C tract insertion/deletion mutations in BHD-affected haplotypecarriers was confirmed by sequencing this amplicon in 30 affected and 28unaffected family members.

A complex mutation, delAGinsC (SEQ ID NO: 3), which resulted in a frameshift and predicted protein truncation 11 missense amino acidsdownstream from the mutation (SEQ ID NO: 4), was identified in Family202 in exon 7 at nt 1087-1088, and was shown to co-segregate withdisease by DHPLC (FIG. 3B).

A 28-bp duplication (nt 1378-1405) was found in exon 9 of affectedmembers of BHD Family 228 (described in Toro et al., J. Med. Genet.39:E10, 2002) (SEQ ID NO: 5), which resulted in wild type and mutantallele size differences that were distinguishable on a 4-20%polyacrylamide gel (FIG. 4). The mutation created a termination codon 79missense amino acids downstream from the end of the duplication (SEQ IDNO: 6).

A fourth mutation was identified in BHD Family 230, a C to Gtransversion at nt 1844 (SEQ ID NO: 11) that produced an in-frametermination at codon 463 in exon 12 (FIG. 3C) (SEQ ID NO: 12).

Each family's mutation was present in affected haplotype carriers withinthat family, but was absent in non-carriers and at least 160 normalindividuals.

TABLE 2 BHD gene mutations in a panel of nine families with BHDsyndrome. Family Exon Mutation^(a) Predicted Result(s) Seq. ID No: 202 71087delAGinsC Frameshift, protein 3 and 4 truncation 228 9 1378→1405dupFrameshift, protein 5 and 6 truncation 174 11 1733insC Frameshift,protein 7 and 8 truncation 200 11 1733insC Frameshift, protein 7 and 8truncation 210 11 1733insC Frameshift, protein 7 and 8 truncation 216 111733insC Frameshift, protein 7 and 8 truncation 201 11 1733delCFrameshift, protein  9 and 10 truncation 230 12 C1844G Tyr463X 11 and 12^(a)Mutations are named according to recommendations of the NomenclatureSystem for Human Gene Mutations. The GenBank mRNA sequence (accessionno. AF517523, SEQ ID NO: 1) of BHD is used for reference. The A of theATG initiator codon is located at nt 456. An additional 14 of 53families had 1733insC, 8 of 53 families had 1733delC, and 2 of 53families had the C1844G mutations.

Fifty-three probands from small BHD families were screened for mutationsin the mononucleotide (C)₈ tract in exon 11 of the BHD gene (FIG. 1). Cinsertions or deletions were found in 22 of the 53 probands, indicatingthat this cytosine mononucleotide tract is hypermutable and particularlyprone to disease-causing mutations. In the examples disclosed herein, atotal of eighteen (C)₉ mutations and nine (C)₇ mutations have beenidentified in 62 BHD patient samples, a (C)₈ tract mutation frequency of44%. Mutations in genes with homonucleotide tracts have been reported inother human disorders, such as NF1 mutations in neurofibromatosis(Rodenhiser et al., Mut. Res. 373:185-195, 1997), BRCA1 mutations inbreast cancer (Rodenhiser et al., Oncogene 12:2623-2629, 1996), and FAAmutations in Fanconi anemia (Levran et al., Proc. Natl. Acad. Sci. USA94:13051-13056, 1997). In addition, mutations in a homonucleotide Gtract in the PAX2 gene have been associated with renal-coloboma syndrome(Schimmenti et al., Human Mutation 14:369-376, 1999). Without beingbound by theory, these mutations are believed to arise through aslippage-mediated mechanism during DNA replication of single baserepeats resulting in expansion or contraction of the homonucleotidetract (Streisinger et al., Symp. Quant. Biol. 31:77-86, 1966). In allcases, these errors result in frameshift mutations leading to proteintruncation.

The disclosed examples of mutations in BHD patients are predicted totruncate the protein, which leads to a loss of function of the BHD geneproduct, folliculin, and to the disease phenotype. If BHD was a classictumor suppressor gene, loss of heterozygosity (LOH) would be expected tooccur in renal tumors from BHD patients. Renal tumors from BHD patientswere evaluated for LOH with polymorphic markers near the BHD gene. LOHwas detected in 15 of 88 (17%) renal tumors from 18 BHD patients,indicating that LOH at the BHD locus is an uncommon second event leadingto tumorigenesis. Alternatively, the inactivation of the second BHDallele may occur by hypermethylation. Haploinsufficiency alone may beenough to produce the BHD phenotype. Another possibility may be that theinactive BHD allele produced by germline mutations results in adominant-negative effect leading to BHD syndrome.

cDNA from adult kidney and adult and fetal lung (Clontech) was used toamplify 3.2 kb of the BHD transcript, which was sequenced to >4-foldcoverage. Separately, a putative full-length clone was obtained byscreening a normal lung cDNA library (Origene Technologies, Inc.) andwas also sequenced to >4-fold coverage. The full length BHD sequence of3674 nucleotides predicted a protein, which we have named folliculin(adapted from the BHD skin lesion, fibrofolliculoma), with an openreading frame of 579 amino acids (FIG. 5B). Programs included in SEQWEBand PROSITE predicted a 64 kDa cytoplasmic protein with a glutamicacid-rich coiled-coil domain, one site of N-glycosylation and threesites of myristylation. Although BLAST alignment against NCBI proteindatabases found no significant homology with any known proteins,folliculin was found to be highly conserved across mammalian species. Byway of example, the mouse ortholog (SEQ ID NO: 15; MGC37841 geneproduct, AAH25820 protein) is 92% identical to human folliculin (SEQ IDNO: 2), illustrating the highly conserved mammalian protein sequence.The Drosophila melanogaster ortholog (CG8616 gene product) is 22-36%identical (44-56% positive) to the human folliculin. Finally, theCaenorhabditis elegans ortholog (F22D3.2 gene product, AAK31497 protein)is 27-28% identical (44-52% positive) to the human folliculin. All ofthese comparisons were measured by BLASTX (Altschul et al., Nuc. AcidRes. 25:3389-3402, 1997) and MAST (Bailey & Gribskov, Bioinformatics14:48-54, 1998). The homologies across species indicate an importantbiological role for folliculin in a wide range of organisms.

Germline mutations in BHD orthologs that map to syntenic locations inthe dog and rat may be responsible for naturally occurring inheritedrenal malignancies in these species, renal cystadenoma anddermatofibroma in German Shepherd dogs (Vilafranca et al., Vet. Pathol.31:713-716, 1994; Jónasdóttir et al., Proc. Nat. Acad. Sci. USA97:4132-4137, 2000) and an inherited renal cancer in the Nihon rat (Hinoet al., Jpn. J. Cancer. Res. 92:1147-1149, 2001). The discovery ofgermline, disease-associated mutations in BHD patients with renalneoplasia and spontaneous pneumothorax underscores the importance of theBHD gene and its product, folliculin, in kidney, lung and skinorganogenesis.

Example 2 BHD Consensus Sequence

A BHD nucleic acid consensus sequence is shown in SEQ ID NO: 42. Thenucleic acid sequence is identical to the wild-type BHD nucleic acidsequence, with the exception of the following nucleic acids:

(a) the M at position 1087 of the consensus sequence can be either an Aor a C,

(b) the N at position 1088 of the consensus sequence can be either a Gor no nucleotide,

(c) the N at position 1388 of the consensus sequence can be either thesequence GTGTTGCCAGAGAGTACAGAAAGCCCCT or no nucleotide,

(d) the N at position 1741 of the consensus sequence can be either a Cor no nucleotide,

(e) the N at position 1742 of the consensus sequence can be either a Cor no nucleotide, and

(f) the S at position 1846 of the consensus sequence can be either a Cor a G.

Example 3 Other BHD Mutations

With the provision herein of the correlation between BHD gene mutationsand BHD syndrome and associated conditions, the isolation andidentification of additional BHD mutations is enabled. Any conventionalmethod for the identification of genetic mutations in a population canbe used to identify such additional mutations.

For instance, existing populations (for example, mouse or humanpopulations) are assessed for symptoms of BHD syndrome, renal neoplasia,and/or spontaneous pneumothorax, and individuals within the populationare genotyped as relates to a BHD sequence. These BHD sequences are thencompared to a reference BHD sequence, such as the wild-type BHD sequence(SEQ ID NO:1), to determine the presence of one or more variantnucleotide positions. Once variant nucleotides are identified,statistical analysis of the population is used to determine whetherthese variants are correlated with BHD syndrome and/or associatedsymptoms.

BHD mutations, for example single nucleotide alterations, can bedetected by a variety of techniques. The techniques used in evaluatingeither somatic or germline single nucleotide alterations includeallele-specific oligonucleotide hybridization (ASOH) (Stoneldng et al.,Am. J. Hum. Genet. 48:370-382, 1991) which involves hybridization ofprobes to the sequence, stringent washing, and signal detection. Othermethods include techniques that incorporate more robust scoring ofhybridization. Examples of these procedures include the ligation chainreaction (ASOH plus selective ligation and amplification), as disclosedin Wu and Wallace (Genomics 4:560-569, 1989); mini-sequencing (ASOH plusa single base extension) as discussed in Syvanen (Meth. Mol. Biol.98:291-298, 1998); and the use of DNA chips (miniaturized ASOH withmultiple oligonucleotide arrays) as disclosed in Lipshutz et al.(BioTechniques 19:442-447, 1995). Alternatively, ASOH with single- ordual-labeled probes can be merged with PCR, as in the 5′-exonucleaseassay (Heid et al., Genome Res. 6:986-994, 1996), or with molecularbeacons (as in Tyagi and Kramer, Nat. Biotechnol. 14:303-308, 1996).

Another technique is dynamic allele-specific hybridization (DASH), whichinvolves dynamic heating and coincident monitoring of DNA denaturation,as disclosed by Howell et al. (Nat. Biotech. 17:87-88, 1999). A targetsequence is amplified by PCR in which one primer is biotinylated. Thebiotinylated product strand is bound to a streptavidin-coated microtiterplate well and the non-biotinylated strand is rinsed away with alkaliwash solution. An oligonucleotide probe, specific for one allele, ishybridized to the target at low temperature. This probe forms a duplexDNA region that interacts with a double strand-specific intercalatingdye. When subsequently excited, the dye emits fluorescence proportionalto the amount of double-stranded DNA (probe-target duplex) present. Thesample is then steadily heated while fluorescence is continuallymonitored. A rapid fall in fluorescence indicates the denaturingtemperature of the probe-target duplex. Using this technique, asingle-base mismatch between the probe and target results in asignificant lowering of melting temperature (Tm) that can be readilydetected.

A variety of other techniques can be used to detect mutations in BHDDNA. Merely by way of example, see U.S. Pat. Nos. 4,666,828; 4,801,531;5,110,920; 5,268,267; 5,387,506; 5,691,153; 5,698,339; 5,736,330;5,834,200; 5,922,542; and 5,998,137 for such methods.

Many mutations can occur in a BHD nucleic acid or amino acid sequencethat do not alter the activity of the protein. For instance, mutationscan appear in a non-coding region of the nucleic acid sequence that donot affect the activity of the folliculin protein, for example innucleic acids 1 through 455 or nucleic acids 2058 through 3674 of SEQ IDNO: 1. In addition, mutations that do not affect folliculin function canoccur in unconserved regions of the BHD amino acid sequence, forexample, in regions in which the human sequence (SEQ ID NO: 2) differsfrom the mouse sequence (SEQ ID NO: 15). These mutations areparticularly unlikely to interfere with folliculin function if they areconservative substitutions. Specific, non-limiting examples of some ofthe regions of SEQ ID NO: 2 that can be mutated without changing proteinfunction include: include mutating amino acid 95 to a leucine; mutatingamino acid 96 to an alanine; mutating amino acid amino acid 100 to aserine; mutating amino acid 101 to a glutamine; mutating amino acid 102to an arginine; mutating amino acid amino 105 to a tyrosine; mutatingamino acid 114 to an alanine; mutating amino acid 115 to a serine;mutating amino acid 116 to a proline; mutating amino acid 120 to avaline; mutating amino acid 121 to an alanine; mutating amino acid 122to a leucine; mutating amino acid 159 to a serine; mutating amino acid160 to a glutamic acid; mutating amino acid 161 to an arginine; mutatingamino acid 168 to a valine; mutating amino acid 169 to a alanine;mutating amino acid 170 to a leucine; mutating amino acid 200 to aserine; mutating amino acid 201 to a glutamic acid; mutating amino acid202 to an arginine; mutating amino acid 261 to a valine; mutating aminoacid 262 to an alanine; mutating amino acid 263 to a leucine; mutatingamino acid 328 to an alanine; mutating amino acid 329 to a serine;mutating amino acid 330 to an asparagine; mutating amino acid 508 to analanine; mutating amino acid 509 to aleucine; mutating amino acid 510 toan alanine; mutating amino acid 561 to an alanine; mutating amino acid562 to an arginine; mutating amino acid 563 to aglycine; mutating aminoacid 564 to an isoleucine; mutating amino acid 565 to a leucine;mutating amino acid 566 to a glutamic acid; mutating amino acid 579 to aserine; mutating amino acid 580 to a glutamic acid; mutating amino acid581 to an arginine; mutating amino acid 591 to an alanine; mutatingamino acid 593 to an alanine; mutating amino acid 600 to a proline;mutating amino acid 601 to a histidine; mutating amino acid 602 to aglutamic acid; mutating amino acid 920 to a threonine; mutating aminoacid 921 to a histidine; mutating amino acid 922 to an arginine;mutating amino acid 928 to a glycine; mutating amino acid 929 to aleucine; mutating amino acid 930 to a tyrosine; mutating amino acid 931to an alanine; mutating amino acid 932 to a leucine; mutating amino acid933 to an alanine; mutating amino acid 952 to aserine; mutating aminoacid 953 to a glutamic acid; mutating amino acid 954 to an arginine;mutating amino acid 955 to acysteine; mutating amino acid 956 to atyrosine; mutating amino acid 957 to a serine; mutating amino acid 960to a threonine; mutating amino acid 961 to a histidine; mutating aminoacid 962 to an arginine; mutating amino acid 972 to a proline; mutatingamino acid 973 to a histidine; mutating amino acid 974 to a glutamicacid; mutating amino acid 981 to an alanine; mutating amino acid 983 toan alanine; mutating amino acid 1001 to a proline; deleting amino acid1003; inserting a threonine following amino acid 1009; mutating aminoacid 1010 to a histidine; mutating amino acid 1012 to a glycine;mutating amino acid 1013 to a leucine; mutating amino acid 1014 to atyrosine; mutating amino acid 1124 to an asparagine; mutating amino acid1131 to a histidine; mutating amino acid 1132 to an isoleucine; mutatingamino acid 1133 to a serine; mutating amino acid 1242 to a proline;mutating amino acid 1243 to an arginine; deleting amino acid 1244;mutating amino acid 1248 to a proline; mutating amino acid 1249 to anarginine; deleting amino acid 1250; mutating amino acid 1256 to analanine; inserting a leucine following amino acid 1256 mutating aminoacid 1257 to an alanine; mutating amino acid 1258 to a histidine;mutating amino acid 1267 to an alanine; mutating amino acid 1268 to aleucine; mutating amino acid 1269 to an alanine; mutating amino acid1279 to a valine; mutating amino acid 1280 to an alanine; mutating aminoacid 1281 to a leucine; mutating amino acid 1285 to a valine; mutatingamino acid 1286 to an alanine; mutating amino acid 1287 to a leucine;mutating amino acid 1300 to a threonine; mutating amino acid 1301 to ahistidine; mutating amino acid 1302 to an arginine; mutating amino acid1306 to a threonine; mutating amino acid 1307 to a histidine; mutatingamino acid 1308 to an arginine; mutating amino acid 1315 to an alanine;mutating amino acid 1316 to a serine; mutating amino acid 1317 to anasparagine; mutating amino acid 1326 to an alanine; mutating amino acid1327 to a leucine; mutating amino acid 1328 to an alanine; mutatingamino acid 1483 to an isoleucine; mutating amino acid 1484 to a leucine;mutating amino acid 1485 to a glutamic acid; mutating amino acid 1581 toa valine; mutating amino acid 1582 to an arginine; mutating amino acid1583 to a leucine; mutating amino acid 1691 to a threonine; mutatingamino acid 1692 to a histidine; mutating amino acid 1703 to a serine;mutating amino acid 1704 to a glutamic acid; and mutating amino acid1705 to an arginine.

Example 4 Clinical Uses of BHD Mutation Sequences

To perform a diagnostic test for the presence or absence of a mutationin a BHD sequence of an individual, a suitable genomic DNA-containingsample from a subject is obtained and the DNA extracted usingconventional techniques. For instance, a blood sample, a buccal swab, ahair follicle preparation, or a nasal aspirate is used as a source ofcells to provide the DNA sample; similarly, a surgical specimen, biopsy,or other biological sample containing genomic DNA is used. It isparticularly contemplated that tumor biopsies (for instance, renal tumorsamples) or tumor DNA found in plasma or other blood products can serveas a source. The extracted DNA is then subjected to in vitroamplification, for example according to standard procedures. The alleleof the single base-pair variant can be determined by conventionalmethods including manual and automated fluorescent DNA sequencing,primer extension methods (Nikiforov, et al., Nucl Acids Res.22:4167-4175, 1994), oligonucleotide ligation assay (OLA) (Nickerson etal., Proc. Natl. Acad. Sci. USA 87:8923-8927, 1990), allele-specific PCRmethods (Rust et al., Nucl. Acids Res. 6:3623-3629, 1993), RNasemismatch cleavage, single strand conformation polymorphism (SSCP),denaturing gradient gel electrophoresis (DGGE), Taq-Man, oligonucleotidehybridization, and the like. Also, see the following U.S. Patents fordescriptions of methods or applications of polymorphism analysis todisease prediction and/or diagnosis: U.S. Pat. No. 4,666,828 (RFLP forHuntington's); U.S. Pat. No. 4,801,531 (prediction of atherosclerosis);U.S. Pat. No. 5,110,920 (HLA typing); U.S. Pat. No. 5,268,267(prediction of small cell carcinoma); and U.S. Pat. No. 5,387,506(prediction of dysautonomia).

Examples of mutations associated with BHD syndrome and/or an increasedlikelihood of spontaneous pneumothorax and/or renal neoplasia are themutations of BID listed in Table 2. The absence of these mutationsindicates a relatively decreased likelihood of having BHD syndrome orrelated symptoms, such as renal neoplasia or spontaneous pneumothorax.In addition to these particular mutations, other sequence variationsthat may be associated with variable predisposition to BHD or likelihoodof having spontaneous pneumothorax and/or renal neoplasia can also bedetected, and used in combination with the disclosed BHD mutations topredict the probability that a subject will tend to develop BHD syndromeor be likely to display spontaneous pneumothorax and/or renal neoplasia.For example, any mutation associated with abnormal expression of thefolliculin protein, such as a truncation, insertion, or deletion. Suchmutations are particularly likely to occur in a mutational “hot spot”that runs from nucleotides 1733 to 1740 of SEQ ID NO:1.

The markers of the present disclosure can be utilized for the detectionof, and differentiation of, individuals who are homozygous andheterozygous for BHD mutations, including the specific mutations listedin Table 2. One value of identifying individuals who carry a diseaseallele of BHD (for example, individuals who are heterozygous orhomozygous for the an allele that contains a BHD disease mutations, suchas any one of those listed in Table 2) is that these individuals canthen initiate or customize therapy to reduce the occurrence of orreverse symptoms of and associated with BHD syndrome, or reduce thelikelihood of developing such symptoms, or undergo more aggressivetreatment of the condition, and thereby beneficially alter its course.In addition, individuals who are heterozygous or homozygous for a BHDmutation can be on the lookout for future developments that may beindicative of developing BHD or a related condition, and for instancemay benefit from heightened screening for spontaneous pneumothorax,renal (or other) neoplasia, and monitoring of possible skin lesions.

Example 5 Gene Probes and Markers

Sequences surrounding and overlapping one or more mutations in the BHDgene can be useful for a number of gene mapping, targeting, anddetection procedures. For example, genetic probes can be readilyprepared for hybridization and detection of a BHD mutation, such as anyone of those listed in Table 2. As will be appreciated, probe sequencesmay be greater than about 10 or more oligonucleotides in length andpossess sufficient complementarity to distinguish between the C (atamino acid residue 1844 in the wildtype allele) and G (in the C1844Gearly truncation mutation, SEQ ID NO: 11), or between the AG atpositions 1087 and 1088 (in the wildtype allele) and the C substitutionat position 1087 (in the 1087delAGinsC mutation, SEQ ID NO: 3).Similarly, sequences surrounding and overlapping any of the specificallydisclosed mutations (or other mutations found in accordance with thepresent teachings), or longer sequences encompassing more than one ofthe specifically disclosed mutations, can be utilized in allele specifichybridization procedures. A similar approach can be adopted to detectother BHD mutations.

Sequences surrounding and overlapping a BHD mutation, or any portion orsubset thereof that allows one to identify the mutation, are highlyuseful. Thus, another embodiment provides a genetic marker predictive ofa mutation involving at least one insertion or deletion in the (C)₈mononucleotide tract at nt residues 1733 through 1740 of BHD (SEQ ID NO:1), comprising a partial sequence of the human BHD gene including atleast about 10 contiguous nucleotide residues that overlap all or aportion of the sequence at residues 1733 through 1740 of the wildtypeBHD or one of the known mutation described herein (for example, 1733insCor 1733delC, SEQ ID NOs: 7 or 9, respectively).

Another specific embodiment is a genetic marker predictive of a mutationof exon 9 of BHD, comprising a partial sequence of the human BHD geneincluding at least about 10 contiguous nucleotide residues that overlapposition 1844 of SEQ ID NO: 1, which position is indicated with thesymbol “N” in the following nucleotide sequence:

GACCAGTCTCTCAGCAAGTANGAGTTTGTGGTGACCAGTGG (residues 1824 to 1864 of SEQID NO: 1), and sequences complementary therewith, wherein “N” representsG (as in the mutant sequence shown in SEQ ID NO: 11) or another singlebase-pair mutation of the C that is present at N in a human allele. Oneexample mutation is a C to G transversion, but can also include a C to Atransversion or C to T transition.

Likewise, another specific embodiment is a genetic marker predictive ofa mutation of exon 9 of BHD, comprising a partial sequence of the humanBHD-encoding sequence including at least about 10 contiguous nucleotideresidues that allow the practitioner to distinguish between the wildtypesequence and a mutation in which residues 1378-1405 of the BHD sequence(SEQ ID NO: 1) are duplicated (as shown in SEQ ID NO: 5). For instance,an oligonucleotide selected from the following sequence, and sequencescomplementary therewith or surrounding at least a portion thereof, suchthat it overlaps a portion of the duplication, can be used to determinewhether a sample comprises the duplication mutation:

AGAAAGCCCCTGTGTTGCCAGAGAGTACAGAAAGCCCCTGTGTTGCCAGAGAGTAC (residues 1378to 1433 of SEQ ID NO: 5.

In each embodiment, longer oligonucleotides are contemplated, that haveat least 11, at least 12, at least 13, at least 14, at least 15, atleast 17, at least 18, at least 20, at least 25, or more contiguousnucleotides. Specific oligonucleotides are about 30, 35, or 40nucleotides in length, or longer. A skilled practitioner will understandhow to select specific oligonucleotide sequences from the providedsequences and the guidance provided herein, in order to generate probesfor determining the presence or absence of any of these markers in abiological sample from a subject, which subject includes nucleic acidsfrom the subjects (either genomic of mRNA nucleic acids, or both).

Example 6 Detecting Nucleotide Variants/Mutations

Many of the mutations that have been detected in the BHD gene thus farhave been frameshift mutations. However, mutations in this gene, such astruncation mutations, also are linked to BHD syndrome and relatedsymptoms, such as spontaneous pneumothorax and/or renal neoplasia. Themutations at nucleotide residue 1844, or 1733, or 1087 and 1088(numbered as in SEQ ID NO: 1), can be detected by a variety oftechniques. These techniques include allele-specific oligonucleotidehybridization (ASOH) (Stoneking et al., Am. J. Hum. Genet. 48:370-382,1991) which involves hybridization of probes to the sequence, stringentwashing, and signal detection. Other new methods include techniques thatincorporate more robust scoring of hybridization Examples of theseprocedures include the ligation chain reaction (ASOH plus selectiveligation and amplification), as disclosed in Wu and Wallace (Genomics4:560-569, 1989); mini-sequencing (ASOH plus a single base extension) asdiscussed in Syvanen (Meth. Mol. Biol. 98:291-298, 1998); and the use ofDNA chips (miniaturized ASOH with multiple oligonucleotide arrays) asdisclosed in Lipshutz et al. (BioTechniques 19:442-447, 1995).Alternatively, ASOH with single- or dual-labeled probes can be mergedwith PCR, as in the 5′-exonuclease assay (Heid et al, Genome Res.6:986-994, 1996), or with molecular beacons (as in Tyagi and Kramer,Nat. Biotechnol. 14:303-308, 1996).

Another technique is dynamic allele-specific hybridization (DASH), whichinvolves dynamic heating and coincident monitoring of DNA denaturation,as disclosed by Howell et al. (Nat. Biotech. 17:87-88, 1999). A targetsequence is amplified by PCR in which one primer is biotinylated. Thebiotinylated product strand is bound to a streptavidin-coated microtiterplate well, and the non-biotinylated strand is rinsed away with alkaliwash solution. An oligonucleotide probe, specific for one allele, ishybridized to the target at low temperature. This probe forms a duplexDNA region that interacts with a double strand-specific intercalatingdye. When subsequently excited, the dye emits fluorescence proportionalto the amount of double-stranded DNA (probe-target duplex) present Thesample is then steadily heated while fluorescence is continuallymonitored. A rapid fall in fluorescence indicates the denaturingtemperature of the probe-target duplex. Using this technique, asingle-base mismatch between the probe and target results in asignificant lowering of melting temperature (T_(m)) that can be readilydetected.

A variety of other techniques can be used to detect point mutations inDNA, which will be appreciated by those of ordinary skill in the artMerely by way of example, see U.S. Pat. Nos. 4,666,828; 4,801,531;5,110,920; 5,268,267; 5,387,506; 5,691,153; 5,698,339; 5,736,330;5,834,200; 5,922,542; and 5,998,137 for such methods.

The nucleotide variants can also be detected using an array of nucleicacid molecules attached to a solid support, in which the array includesan oligonucleotide that hybridizes to a nucleic acid molecule thatcontains a mutation associated with abnormal expression of thefolliculin molecule, such as the mutations shown in SEQ ID NOs: 3, 5, 7,9, and 11. Hybridization is performed under conditions in which theoligonucleotide will hybridize to the mutant sequence but not to thewild-type sequence (SEQ ID NO:1). Examples of patents that disclose howto make and use such arrays include U.S. Pat. Nos. 6,344,316 and6,551,784.

Example 7 Detection of BHD Nucleic Acid Level(s)

Individuals carrying mutations in the BHD gene, or having amplificationsor heterozygous or homozygous deletions of the BHD gene, may be detectedat the DNA or RNA level with the use of a variety of techniques. Thedetection of mutations was discussed above; in the following example,techniques are provided for detecting the level of BHD nucleic acidmolecules in a sample.

For such diagnostic procedures, a biological sample of the subject (ananimal, such as a mouse or a human), which biological sample containseither DNA or RNA derived from the subject, is assayed for a mutated,amplified or deleted BHD encoding sequence, such as a genomicamplification of the BHD gene or an over- or under-abundance of a BHDmRNA. Suitable biological samples include samples containing genomic DNAor mRNA obtained from, for instance, subject body cells, such as thosepresent in peripheral blood, urine, saliva, tissue biopsy, surgicalspecimen, amniocentesis samples and autopsy material. The detection inthe biological sample of a mutant BHD gene, a mutant or truncated BBDRNA, or an amplified or homozygously or heterozygously deleted BHD gene,may be performed by a number of methodologies.

Gene dosage (copy number) can be important in disease states, and caninfluence mRNA and thereby protein level; it is therefore advantageousto determine the number of copies of BHD nucleic acids in samples oftissue. Probes generated from the encoding sequence of BHD (BHD probesor primers) can be used to investigate and measure genomic dosage of theBHD gene.

Techniques for measuring gene dosage are known in the art; see forinstance, U.S. Pat. No. 5,569,753 (“Cancer Detection Probes”) and Pinkelet al. (Nat. Genet. 20:207-211, 1998) (“High Resolution Analysis of DNACopy Number Variation using Comparative Genomic Hybridization toMicroarrays”).

Determination of gene copy number in cells of a patient-derived sampleusing other techniques is known in the art. For example, BHDamplification in immortalized cell lines as well as uncultured cellstaken from a subject can be carried out using bicolor FISH analysis. Byway of example, interphase FISH analysis of immortalized cell lines canbe carried out as previously described (Barlund et al., Genes Chromo.Cancer 20:372-376, 1997). The hybridizations can be evaluated using aZeiss or other fluorescence microscope. By way of example, approximately20 non-overlapping nuclei with intact morphology based on DAPIcounterstain are scored to determine the mean number of hybridizationsignals for each test and reference probe.

Likewise, FISH can be performed on tissue microarrays, as described inKononen et al. (Nat. Med. 4:844-847, 1998). Briefly, consecutivesections of the array are deparaffinized, dehydrated in ethanol,denatured at 74° C. for 5 minutes in 70% formamide/2×SSC, and hybridizedwith test and reference probes. The specimens containing tight clustersof signals or >3-fold increase in the number of test probe as comparedto chromosome 17 centromere in at least 10% of the tumor cells may beconsidered as amplified. Microarrays using various tissues can beconstructed as described in WO9944063A2 and WO9944062A1.

Overexpression of the BHD gene can also be detected by measuring thecellular level of BHD-specific mRNA. mRNA can be measured usingtechniques well known to those of ordinary skill in the art, includingfor instance Northern analysis, RT-PCR and mRNA in situ hybridization.

Example 8 Methods of Making Human BHD cDNA

The original means by which the wildtype and mutant BHD cDNAs wereidentified and obtained is described above. With the provision of thesequence of the folliculin proteins (SEQ ID NOs: 2, 4, 6, 8, and 12) andcDNA (SEQ ID NOs: 1, 3, 5, 7, 9, and 11), in vitro nucleic acidamplification (such as polymerase chain reaction (PCR)) now may beutilized in a simple method for producing BHD cDNA. The followingexample provides techniques for preparing cDNA in this manner.

Total RNA is extracted from human cells by any one of a variety ofmethods well known to those of ordinary skill in the art. Sambrook etal. (In Molecular Cloning: A Laboratory Manual, CSHL, New York, 1989)and Ausubel et al. (In Current Protocols in Molecular Biology, GreenePubl. Assoc. and Wiley-Intersciences, 1992) provide descriptions ofmethods for RNA isolation. Because BHD is expressed in tumors and innormal tissue, human cell lines derived from tumors or normal tissue canbe used as a source of such RNA. The extracted RNA is then used as atemplate for performing reverse transcription-polymerase chain reaction(RT-PCR) amplification of cDNA. Methods and conditions for RT-PCR aredescribed in Kawasali et al., (In PCR Protocols, A Guide to Methods andApplications, Innis et al. (eds.), 21-27, Academic Press, Inc., SanDiego, Calif., 1990).

The selection of amplification primers will be made according to theportion(s) of the cDNA that is to be amplified. Primers may be chosen toamplify a segment of a cDNA or the entire cDNA molecule. Variations inamplification conditions may be required to accommodate primers andamplicons of differing lengths and composition; such considerations arewell known in the art and are discussed for instance in Innis et al.(PCR Protocols, A Guide to Methods and Applications, Academic Press,Inc., San Diego, Calif., 1990). By way of example, the portions of thehuman BHD cDNA molecule may be amplified using the combination ofprimers discussed above, in Example 1. These primers are illustrativeonly; one skilled in the art will appreciate that many different primersmay be derived from the provided cDNA sequence in order to amplifyparticular regions of BHD cDNA, as well as the complete sequence of thehuman BHD cDNA.

Re-sequencing of PCR products obtained by these amplification proceduresis advantageous to facilitate confirmation of the amplified sequence andprovide information about natural variation of this sequence indifferent populations or species. Oligonucleotides derived from theprovided BHD sequences may be used in such sequencing methods.

Orthologs of human BHD can be cloned in a similar manner, where thestarting material consists of cells taken from a non-human species.Orthologs will generally share at least 20% sequence identity with thedisclosed human BHD cDNA, while exhibiting substantially greatersequence identity at the protein level due to the wobble effect. Wherethe non-human species is more closely related to humans, the sequenceidentity will in general be greater. Closely related orthologous BHDmolecules may share at least 70%, at least 75%, at least 80% at least85%, at least 90%, at least 91%, at least 93%, at least 95%, or at least98% sequence identity with the disclosed human sequences.

Oligonucleotides derived from the human BHD cDNA, or fragments of thiscDNA, are encompassed within the scope of the present disclosure. Sucholigonucleotides may comprise a sequence of at least 15 consecutivenucleotides of the BHD nucleic acid sequence. If these oligonucleotidesare used with an in vitro amplification procedure (such as PCR),lengthening the oligonucleotides may enhance amplification specificity.Thus, oligonucleotide primers comprising at least 25, 30, 35, 40, 45, or50 consecutive nucleotides of these sequences may be used. These primersfor instance may be obtained from any region of the disclosed sequences.By way of example, the human BHD cDNA, ORF and gene sequences may beapportioned into about halves or quarters based on sequence length, andthe isolated nucleic acid molecules (for example, oligonucleotides) maybe derived from the first or second halves of the molecules, or any ofthe four quarters.

Nucleic acid molecules may be selected that comprise at least 15, 20,23, 25, 30, 35, 40, 50, or 100 consecutive nucleotides of any of theseor other portions of the human BHD cDNA. Thus, representative nucleicacid molecules might comprise at least 15 consecutive nucleotides of thehuman BHD cDNA (SEQ ID NO: 1).

Example 9 BHD Sequence Variants

With the provision of human BHD protein (folliculin) and correspondingnucleic acid sequences herein, both wildtype and various mutants, thecreation of variants of these sequences is now enabled.

Variant folliculin proteins include proteins that differ in amino acidsequence from the human folliculin sequences disclosed but that share atleast 60% amino acid sequence identity with the provided humanfolliculin protein. Other variants will share at least 75%, at least80%, at least 85%, at least 90%, at least 95%, or at least 98% aminoacid sequence identity. Manipulation of the nucleotide sequence of BHDusing standard procedures, including for instance site-directedmutagenesis or PCR, can be used to produce such variants. The simplestmodifications involve the substitution of one or more amino acids foramino acids having similar biochemical properties. These conservativesubstitutions are likely to have minimal impact on the activity of theresultant protein. Table 3 shows amino acids that may be substituted foran original amino acid in a protein, and which are regarded asconservative substitutions.

TABLE 3 Original Residue Conservative Substitutions Ala ser Arg lys Asngln; his Asp glu Cys ser Gln asn Glu asp Gly pro His asn; gln Ile leu;val Leu ile; val Lys arg; gln; glu Met leu; ile Phe met; leu; tyr Serthr Thr ser Trp tyr Tyr trp; phe Val ile; leu

More substantial changes in enzymatic function or other protein featuresmay be obtained by selecting amino acid substitutions that are lessconservative than those listed in Table 3. Such changes include changingresidues that differ more significantly in their effect on maintainingpolypeptide backbone structure (for example, sheet or helicalconformation) near the substitution, charge or hydrophobicity of themolecule at the target site, or bulk of a specific side chain. Thefollowing substitutions are generally expected to produce the greatestchanges in protein properties: (a) a hydrophilic residue (for example,seryl or threonyl) is substituted for (or by) a hydrophobic residue (forexample, leucyl, isoleucyl, phenylalanyl, valyl or alanyl); (b) acysteine or proline is substituted for (or by) any other residue; (c) aresidue having an electropositive side chain (for example, lysyl,arginyl, or histadyl) is substituted for (or by) an electronegativeresidue (for example, glutamyl or aspartyl); or (d) a residue having abulky side chain (for example, phenylalanine) is substituted for (or by)one lacking a side chain (for example, glycine).

Variant folliculin encoding sequences may be produced by standard DNAmutagenesis techniques, for example, M13 primer mutagenesis. Details ofthese techniques are provided in Sambrook et al. (In Molecular Cloning:A Laboratory Manual, CSHL, New York, 1989), Ch. 15. By the use of suchtechniques, variants may be created that differ in minor ways from thehuman folliculin sequences disclosed. DNA molecules and nucleotidesequences that are derivatives of those specifically disclosed herein,and which differ from those disclosed by the deletion, addition, orsubstitution of nucleotides while still encoding a protein that has atleast 60% sequence identity with the human folliculin encoding sequencedisclosed (SEQ ID NO: 1), are comprehended by this disclosure. Alsocomprehended are more closely related nucleic acid molecules that shareat least 70%, at least 75%, at least 80%, at least 85%, at least 90%, atleast 95%, or at least 98% nucleotide sequence identity with thedisclosed folliculin sequences. In their most simple form, such variantsmay differ from the disclosed sequences by alteration of the codingregion to fit the codon usage bias of the particular organism into whichthe molecule is to be introduced.

Alternatively, the coding region may be altered by taking advantage ofthe degeneracy of the genetic code to alter the coding sequence suchthat, while the nucleotide sequence is substantially altered, itnevertheless encodes a protein having an amino acid sequencesubstantially similar to the disclosed human folliculin proteinsequences. For example, because of the degeneracy of the genetic code,four nucleotide codon triplets—(GCT, GCG, GCC and GCA)—code for alanine.The coding sequence of any specific alanine residue within the humanfolliculin protein, therefore, could be changed to any of thesealternative codons without affecting the amino acid composition orcharacteristics of the encoded protein. Based upon the degeneracy of thegenetic code, variant DNA molecules may be derived from the cDNA andgene sequences disclosed herein using standard DNA mutagenesistechniques as described above, or by synthesis of DNA sequences. Thus,this disclosure also encompasses nucleic acid sequences that encode afolliculin protein, but which vary from the disclosed nucleic acidsequences by virtue of the degeneracy of the genetic code.

Variants of the folliculin protein may also be defined in terms of theirsequence identity with the prototype human folliculin protein (SEQ IDNO: 2). As described above, folliculin proteins share at least 60%, atleast 75%, at least 80%, at least 85%, at least 90%, at least 95%, or atleast 98% amino acid sequence identity with the human folliculin protein(SEQ ID NO: 2). Nucleic acid sequences that encode suchproteins/fragments readily may be determined simply by applying thegenetic code to the amino acid sequence of a folliculin protein orfragment, and such nucleic acid molecules may readily be produced byassembling oligonucleotides corresponding to portions of the sequence.

Nucleic acid molecules that are derived from the human BHD cDNA nucleicacid sequences include molecules that hybridize under stringentconditions to the disclosed prototypical BHD nucleic acid molecules, orfragments thereof. In particular embodiments, the nucleic acid moleculeor fragments hybridize under conditions of low stringency, highstringency, or very high stringency as defined above.

Human BHD nucleic acid encoding molecules (including the cDNA shown inSEQ ID NOs: 1, 3, 5, 7, 9, and 11, and nucleic acids comprising thissequence), and orthologs and homologs of these sequences, may beincorporated into transformation or expression vectors.

Example 10 Expression of Folliculins

The expression and purification of proteins, such as the BHD protein,folliculin, can be performed using standard laboratory techniques. Afterexpression, purified BHD protein may be used for functional analyses,antibody production, diagnostics, and patient therapy. Furthermore, theDNA sequence of the BHD cDNA can be manipulated in studies to understandthe expression of the gene and the function of its product. Mutant formsof the human BHD gene may be isolated based upon information containedherein, and may be studied in order to detect alteration in expressionpatterns in terms of relative quantities, tissue specificity, andfunctional properties of the encoded mutant BHD protein. Partial orfull-length cDNA sequences, which encode for the subject protein, may beligated into bacterial expression vectors. Methods for expressing largeamounts of protein from a cloned gene introduced into Escherichia coli(E. coli) may be utilized for the purification, localization, andfunctional analysis of proteins. For example, fusion proteins consistingof amino terminal peptides encoded by a portion of the E. coli lacZ ortrpE gene linked to BHD proteins (folliculins) may be used to preparepolyclonal and monoclonal antibodies against these proteins. Thereafter,these antibodies may be used to purify proteins by immunoaffinitychromatography, in diagnostic assays to quantitate the levels of proteinand to localize proteins in tissues and individual cells byimmunofluorescence. Similarly, fusion proteins comprising folliculin ora fragment thereof may also be generated for use as fusion proteins,depending on the peptide or protein to which the folliculin is linked.The construction and use of fusion proteins is generally known to thoseof ordinary skill.

Intact native protein may also be produced in E. coli in large amountsfor functional studies. Methods and plasmid vectors for producing fusionproteins and intact native proteins in bacteria are described inSambrook et al. (In Molecular Cloning: A Laboratory Manual, Ch. 17,CSHL, New York, 1989). Such fusion proteins may be made in largeamounts, are easy to purify, and can be used to elicit antibodyresponse. Native proteins can be produced in bacteria by placing astrong, regulated promoter and an efficient ribosome-binding siteupstream of the cloned gene. If low levels of protein are produced,additional steps may be taken to increase protein production; if highlevels of protein are produced, purification is relatively easy.Suitable methods are presented in Sambrook et al. (In Molecular Cloning:A Laboratory Manual, CSHL, New York, 1989) and are well known in theart. Often, proteins expressed at high levels are found in insolubleinclusion bodies. Methods for extracting proteins from these aggregatesare described by Sambrook et al. (In Molecular Cloning: A LaboratoryManual, Ch. 17, CSHL, New York, 1989). Vector systems suitable for theexpression of lacZ fusion genes include the pUR series of vectors(Ruther and Muller-Hill, EMBO J. 2:1791, 1983), pEX1-3 (Stanley andLuzio, EMBO J. 3:1429, 1984) and pMR100 (Gray et al., Proc. Natl. Acad.Sci. USA 79:6598, 1982). Vectors suitable for the production of intactnative proteins include pKC30 (Shimatake and Rosenberg, Nature 292:128,1981), pKK177-3 (Amann and Brosius, Gene 40:183, 1985) and pET-3(Studiar and Moffatt, J. Mol. Biol. 189:113, 1986). BHD fusion proteinsmay be isolated from protein gels, lyophilized, ground into a powder,and used as an antigen. The DNA sequence can also be transferred fromits existing context to other cloning vehicles, such as other plasmids,bacteriophages, cosmids, animal viruses and yeast artificial chromosomes(YACs) (Burke et al, Science 236:806-812, 1987). These vectors may thenbe introduced into a variety of hosts including somatic cells, andsimple or complex organisms, such as bacteria, fingi (Timberlake andMarshall, Science 244:1313-1317, 1989), invertebrates, plants (Gasserand Fraley, Science 244:1293, 1989), and animals (Pursel et al., Science244:1281-1288, 1989), which cell or organisms are rendered transgenic bythe introduction of the heterologous BHD cDNA.

For expression in mammalian cells, the cDNA sequence may be ligated toheterologous promoters, such as the simian virus (SV) 40 promoter in thepSV2 vector (Mulligan and Berg, Proc. Natl. Acad. Sci. USA 78:2072-2076,1981), and introduced into cells, such as monkey COS-1 cells (Gluzman,Cell 23:175-182, 1981), to achieve transient or long-term expression.The stable integration of the chimeric gene construct may be maintainedin mammalian cells by biochemical selection, such as neomycin (Southernand Berg, J. Mol. Appl. Genet. 1:327-341, 1982) and mycophenolic acid(Mulligan and Berg, Proc. Natl. Acad. Sci. USA 78:2072-2076, 1981).

DNA sequences can be manipulated with standard procedures such asrestriction enzyme digestion, fill-in with DNA polymerase, deletion byexonuclease, extension by terminal deoxynucleotide transferase, ligationof synthetic or cloned DNA sequences, site-directed sequence-alterationvia single-stranded bacteriophage intermediate or with the use ofspecific oligonucleotides in combination with PCR.

The cDNA sequence (or portions derived from it) or a mini gene (a cDNAwith an intron and its own promoter) may be introduced into eukaryoticexpression vectors by conventional techniques. These vectors aredesigned to permit the transcription of the cDNA in eukaryotic cells byproviding regulatory sequences that initiate and enhance thetranscription of the cDNA and ensure its proper splicing andpolyadenylation. Vectors containing the promoter and enhancer regions ofthe SV40 or long terminal repeat (LTR) of the Rous Sarcoma virus andpolyadenylation and splicing signal from SV40 are readily available(Mulligan et al., Proc. Natl. Acad. Sci. USA 78:1078-2076, 1981; Gormanet al., Proc. Natl. Acad. Sci USA 78:6777-6781, 1982). The level ofexpression of the cDNA can be manipulated with this type of vector,either by using promoters that have different activities (for example,the baculovirus pAC373 can express cDNAs at high levels in S. frugiperdacells (Summers and Smith, In Genetically Altered Viruses and theEnvironment, Fields et al. (Eds.) 22:319-328, CSHL Press, Cold SpringHarbor, N.Y., 1985) or by using vectors that contain promoters amenableto modulation, for example, the glucocorticoid-responsive promoter fromthe mouse mammary tumor virus (Lee et al., Nature 294:228, 1982). Theexpression of the cDNA can be monitored in the recipient cells 24 to 72hours after introduction (transient expression).

In addition, some vectors contain selectable markers such as the gpt(Mulligan and Berg, Proc. Natl. Acad. Sci. USA 78:2072-2076, 1981) orneo (Southern and Berg, J. Mol. Appl. Genet. 1:327-341, 1982) bacterialgenes. These selectable markers permit selection of transfected cellsthat exhibit stable, long-term expression of the vectors (and thereforethe cDNA). The vectors can be maintained in the cells as episomal,freely replicating entities by using regulatory elements of viruses suchas papilloma (Sarver et al., Mol. Cell Biol. 1:486, 1981) orEpstein-Barr (Sugden et al., Mol. Cell Biol. 5:410, 1985).Alternatively, one can also produce cell lines that have integrated thevector into genomic DNA. Both of these types of cell lines produce thegene product on a continuous basis. One can also produce cell lines thathave amplified the number of copies of the vector (and therefore of thecDNA as well) to create cell lines that can produce high levels of thegene product (Alt et al., J. Biol. Chem. 253:1357, 1978).

The transfer of DNA into eukaryotic, in particular human or othermammalian cells, is now a conventional technique. The vectors areintroduced into the recipient cells as pure DNA (transfection) by, forexample, precipitation with calcium phosphate (Graham and vander Eb,Virology 52:466, 1973) or strontium phosphate (Brash et al., Mol. CellBiol. 7:2013, 1987), electroporation (Neumann et al., EMBO J. 1:841,1982), lipofection (Felgner et al., Proc. Natl. Acad Sci USA 84:7413,1987), DEAE dextran (McCuthan et al., J. Natl. Cancer Inst. 41:351,1968), microinjection (Mueller et al., Cell 15:579, 1978), protoplastfusion (Schafner, Proc. Natl. Acad. Sci. USA 77:2163-2167, 1980), orpellet guns (Klein et al., Nature 327:70, 1987). Alternatively, thecDNA, or fragments thereof, can be introduced by infection with virusvectors. Systems are developed that use, for example, retroviruses(Bernstein et al., Gen. Engr'g 7:235, 1985), adenoviruses (Ahmad et al.,J. Virol. 57:267, 1986), or Herpes virus (Spaete et al., Cell 30:295,1982). BHD encoding sequences can also be delivered to target cells invitro via non-infectious systems, for instance liposomes.

These eukaryotic expression systems can be used for studies offolliculin-encoding nucleic acids and mutant forms of these molecules,the folliculin protein, and mutant forms of this protein. Such usesinclude, for example, the identification of regulatory elements locatedin the 5′ region of the BHD gene on genomic clones that can be isolatedfrom human genomic DNA libraries using the information contained in thepresent disclosure. The eukaryotic expression systems may also be usedto study the function of the normal complete protein, specific portionsof the protein, or of naturally occurring or artificially producedmutant proteins.

Using the above techniques, the expression vectors containing the BHDgene sequence or cDNA, or fragments or variants or mutants thereof, canbe introduced into human cells, mammalian cells from other species, ornon-mammalian cells as desired. The choice of cell is determined by thepurpose of the treatment. For example, monkey COS cells (Gluzman, Cell23:175-182, 1981) that produce high levels of the SV40 T antigen andpermit the replication of vectors containing the SV40 origin ofreplication may be used. Similarly, Chinese hamster ovary (CHO), mouseNIH 3T3 fibroblasts or human fibroblasts or lymphoblasts may be used.

The present disclosure thus encompasses recombinant vectors thatcomprise all or part of the BHD gene or cDNA sequences, for expressionin a suitable host. The BHD DNA is operatively linked in the vector toan expression control sequence in the recombinant DNA molecule so thatthe folliculin polypeptide can be expressed. The expression controlsequence may be selected from the group consisting of sequences thatcontrol the expression of genes of prokaryotic or eukaryotic cells andtheir viruses and combinations thereof. The expression control sequencemay be specifically selected from the group consisting of the lacsystem, the trp system, the lac system, the trc system, major operatorand promoter regions of phage lambda, the control region of fd coatprotein, the early and late promoters of SV40, promoters derived frompolyoma, adenovirus, retrovirus, baculovirus and simian virus, thepromoter for 3-phosphoglycerate kinase, the promoters of yeast acidphosphatase, the promoter of the yeast alpha-mating factors andcombinations thereof.

The host cell, which may be transfected with the vector of thisdisclosure, may be selected from the group consisting of E. coli,Pseudomonas, Bacillus subtilis, Bacillus stearothermophilus or otherbacilli; other bacteria; yeast; fungi; insect; mouse or other animal; orplant hosts; or human tissue cells.

It is appreciated that for mutant or variant BHD DNA sequences, similarsystems are employed to express and produce the mutant product. Inaddition, fragments of the BHD protein can be expressed essentially asdetailed above. Such fragments include individual BHD protein domains orsub-domains, as well as shorter fragments such as peptides. BHD proteinfragments having therapeutic properties may be expressed in this manneralso.

Example 11 Production of BHD (Folliculin) Protein Specific BindingAgents

Monoclonal or polyclonal antibodies may be produced to either the normalBHD (folliculin) protein or mutant forms of this protein. For instance,antibodies may be produced that recognize a mutant BHD protein but failto recognize a wild-type BHD protein, or which recognize a wild-type BHDprotein, but fail to recognize a mutant BHD protein (see below).Optimally, antibodies raised against these proteins or peptides wouldspecifically detect the protein or peptide with which the antibodies aregenerated. That is, an antibody generated to the BHD protein or afragment thereof would recognize and bind the BHD protein and would notsubstantially recognize or bind to other proteins found in human cells.

The determination that an antibody specifically detects the BHD proteinis made by any one of a number of standard immunoassay methods; forinstance, the Western blotting technique (Sambrook et al., In MolecularCloning: A Laboratory Manual, CSHL, New York, 1989). To determine that agiven antibody preparation (such as one produced in a mouse)specifically detects the BHD protein by Western blotting, total cellularprotein is extracted from human cells (for example, lymphocytes) andelectrophoresed on a sodium dodecyl sulfate-polyacrylamide gel. Theproteins are then transferred to a membrane (for example,nitrocellulose) by Western blotting, and the antibody preparation isincubated with the membrane. After washing the membrane to removenon-specifically bound antibodies, the presence of specifically boundantibodies is detected by the use of an anti-mouse antibody conjugatedto an enzyme such as alkaline phosphatase. Application of an alkalinephosphatase substrate 5-bromo-4-chloro-3-indolyl phosphate/nitro bluetetrazolium results in the production of a dense blue compound byimmunolocalized alkaline phosphatase. Antibodies that specificallydetect the BHD protein will, by this technique, be shown to bind to theBHD protein band (which will be localized at a given position on the geldetermined by its molecular weight). Non-specific binding of theantibody to other proteins may occur and may be detectable as a weaksignal on the Western blot. The non-specific nature of this binding willbe recognized by one skilled in the art by the weak signal obtained onthe Western blot relative to the strong primary signal arising from thespecific antibody-BHD protein binding.

Substantially pure BHD protein or protein fragment peptide) suitable foruse as an immunogen may be isolated from the transfected or transformedcells as described above. Concentration of protein or peptide in thefinal preparation is adjusted, for example, by concentration on anAmicon filter device, to the level of a few micrograms per milliliter.Monoclonal or polyclonal antibody to the protein can then be prepared asfollows:

A. Monoclonal Antibody Production by Hybridoma Fusion

Monoclonal antibody to epitopes of the BHD protein identified andisolated as described can be prepared from murine hybridomas accordingto the classical method of Kohler and Milstein (Nature 256:495-497,1975) or derivative methods thereof. Briefly, a mouse is repetitivelyinoculated with a few micrograms of the selected protein over a periodof a few weeks. The mouse is then sacrificed, and the antibody-producingcells of the spleen isolated. The spleen cells are fused by means ofpolyethylene glycol with mouse myeloma cells, and the excess un-fusedcells destroyed by growth of the system on selective media comprisingaminopterin (HAT media). The successfully fused cells are diluted andaliquots of the dilution placed in wells of a microtiter plate wheregrowth of the culture is continued. Antibody-producing clones areidentified by detection of antibody in the supernatant fluid of thewells by immunoassay procedures, such as ELISA, as originally describedby Engvall (Meth. Enzymol. 70:419-39, 1980), and derivative methodsthereof. Selected positive clones can be expanded and their monoclonalantibody product harvested for use. Detailed procedures for monoclonalantibody production are described in Harlow and Lane (Antibodies, ALaboratory Manual, CSHL, New York, 1988).

B. Polyclonal Antibody Production by Immunization

Polyclonal antiserum containing antibodies to heterogeneous epitopes ofa single protein can be prepared by immunizing suitable animals with theexpressed protein (Example 9), which can be unmodified or modified toenhance immunogenicity. Effective polyclonal antibody production isaffected by many factors related both to the antigen and the hostspecies. For example, small molecules tend to be less immunogenic thanothers and may require the use of carriers and adjuvant. Also, hostanimals vary in response to site of inoculations and dose, with eitherinadequate or excessive doses of antigen resulting in low titerantisera. Small doses (ng level) of antigen administered at multipleintradermal sites appear to be most reliable. An effective immunizationprotocol for rabbits can be found in Vaitukaitis et al. (J. Clin.Endocrinol. Metab. 33:988-991, 1971).

Booster injections can be given at regular intervals, and antiserumharvested when antibody titer thereof, as determinedsemi-quantitatively, for example, by double immunodiffusion in agaragainst known concentrations of the antigen, begins to fall. See, forexample, Ouchterlony et at (In Handbook of Experimental Immunology,Wier, D. (ed.) chapter 19. Blackwell, 1973). Plateau concentration ofantibody is usually in the range of about 0.1 to 0.2 mg/ml of serum(about 12 ?M). Affinity of the antisera for the antigen is determined bypreparing competitive binding curves, as described, for example, byFisher (Manual of Clinical Immunology, Ch. 42, 1980).

C. Antibodies Raised against Synthetic Peptides

A third approach to raising antibodies against the BHD protein orpeptides is to use one or more synthetic peptides synthesized on acommercially available peptide synthesizer based upon the predictedamino acid sequence of the BHD protein or peptide. Polyclonal antibodiescan be generated by injecting these peptides into, for instance,rabbits.

D. Antibodies Raised by Injection of BHD Encoding Sequence

Antibodies may be raised against BHD proteins and peptides bysubcutaneous injection of a DNA vector that expresses the desiredprotein or peptide, or a fragment thereof, into laboratory animals, suchas mice. Delivery of the recombinant vector into the animals may beachieved using a hand-held form of the Biolistic system (Sanford et al,Particulate Sci. Technol. 5:27-37, 1987) as described by Tang et al(Nature 356:152-154, 1992). Expression vectors suitable for this purposemay include those that express the BHD encoding sequence under thetranscriptional control of either the human beta-actin promoter or thecytomegalovirus (CMV) promoter.

Antibody preparations prepared according to these protocols are usefulin quantitative immunoassays which determine concentrations ofantigen-bearing substances in biological samples; they are also usedsemi-quantitatively or qualitatively to identify the presence of antigenin a biological sample; or for immunolocalization of the BHD protein.

For administration to human patients, antibodies, for example,BHD-specific monoclonal antibodies, can be humanized by methods known inthe art. Antibodies with a desired binding specificity can becommercially humanized (Scotgene, Scotland, UK; Oxford Molecular, PaloAlto, Calif.).

E. Antibodies Specific for Mutant Folliculin

With the provision of several inactivating mutant folliculin proteins,the production of antibodies that specifically recognize these proteins(and peptides derived therefrom) is enabled. In particular, productionof antibodies (and fragments and engineered versions thereof) thatrecognize at least one folliculin variant with a higher affinity thanthey recognize wild type folliculin is beneficial, as the resultantantibodies can be used in diagnosis and treatment, as well as in studyand examination of the folliculin proteins themselves.

In particular embodiments, it is beneficial to generate antibodies froma peptide taken from a mutation or variation-specific region of thefolliculin protein. By way of example, such regions include a portion orall of exon 7, exon 9, exon 11, or exon 12 of BHD protein (folliculin).More particularly, it is beneficial to raise antibodies against peptidesof four or more contiguous amino acids that overlap the mutationsidentified in SEQ ID NO: 4, 6, 8, 10, or 12, and particularly whichcomprise at least four contiguous amino acids including the residue(s)shown in positions 211-221 of SEQ ID NO: 4, positions 303-397 of SEQ IDNO: 6, positions 429-454 of SEQ ID NO: 8, positions 429-466 of SEQ IDNO: 10, or position 463 of SEQ ID NO: 12.

Longer peptides also can be used, and in some instances will produce astronger or more reliable immunogenic response. Thus, it is contemplatedin some embodiments that more than 4 amino acids are used to elicit theimmune response, for instance, at least 5, at least 6, at least 8, atleast 10, at least 12, at least 15, at least 18, at least 20, at least25, or more, such as 30, 40, 50, or even longer peptides. Also, it willbe understood by those of ordinary skill that it is beneficial in someinstances to include adjuvants and other immune response enhancers,including passenger peptides or proteins, when using peptides to inducean immune response for production of antibodies.

Embodiments are not limited to antibodies that recognize epitopescontaining the actual mutation identified in each variant. Instead, itis contemplated that variant-specific antibodies also may each recognizean epitope located anywhere throughout the folliculin variant molecule,which epitopes are changed in conformation and/or availability becauseof the activating mutation. Antibodies directed to any of thesevariant-specific epitopes are also encompassed herein.

By way of example, the following references provide descriptions ofmethods for making antibodies specific to mutant proteins: Hills et al.,(Specific targeting of a mutant, activated EGF receptor found inglioblastoma using a monoclonal antibody. Int. J. Cancer, 63: 537-543,1995); Reiter & Maihle (A 1.8 kb alternative transcript from the humanepidermal growth factor receptor gene encodes a truncated form of thereceptor. Nucleic Acids Res., 24: 4050-4056, 1996); Okamoto et al.(Monoclonal antibody against the fusion junction of a deletion-mutantepidermal growth factor receptor. Br. J. Cancer, 73: 1366-1372, 1996);Nakayashiki et al., (Production of a single-chain variable fragmentantibody recognizing type m mutant epidermal growth factor receptor.Jpn. J. Cancer Res., 91: 1035-1043, 2000); Gannon et al. (Activatingmutations in p53 produce a common conformational effect A monoclonalantibody specific for the mutant form. EMBO J., 9: 1595-1602, 1990);Wong et al. (Detection of activated Mr 21,000 protein, the product ofras oncogenes, using antibodies with specificity for amino acid 12.Cancer Res., 46: 6029-6033, 1986); and Carney et al. (A monoclonalantibody reactive with an activated ras protein expressing valine atposition 12. J Cell Biochem., 32: 207-214, 1986). Similar methods can beemployed to generate antibodies specific to specific BHD protein(folliculin) variants.

Example 12 Protein-Based Diagnosis

An alternative method of detecting BHD gene amplification, deletion ormutation, as well as abnormal BHD expression, is to quantitate the levelof BHD protein (folliculin) in the cells of an individual, or toquantitate the level of truncated BHD protein and/or the full length BHDprotein. This diagnostic tool would be useful for detecting reducedlevels of the BHD protein that result from, for example, mutations inthe promoter regions of the BHD gene or mutations within the codingregion of the gene that produced truncated, non-functional or unstablepolypeptides, as well as from deletions of a portion of or the entireBHD gene. Alternatively, duplications of a BHD encoding sequence may bedetected as an increase in the expression level of BHD protein. Such anincrease in protein expression may also be a result of an up-regulatingmutation in the promoter region or other regulatory or coding sequencewithin the BHD gene.

Localization and/or coordinated BHD expression (temporally or spatially)can also be examined using known techniques, such as isolation andcomparison of BHD from cell or tissue specific, or time specific,samples. The determination of reduced or increased BHD protein levels,in comparison to such expression in a control cell (for example, normal,as in taken from a subject not suffering from BHD syndrome or relatedsymptoms), would be an alternative or supplemental approach to thedirect determination of BHD gene deletion, amplification or mutationstatus by the methods disclosed herein and equivalents.

The availability of antibodies specific to the BHD protein facilitatesthe detection and quantitation of cellular BHD by one of a number ofimmunoassay methods which are well known in the art and are presented inHarlow and Lane (Antibodies, A Laboratory Manual, CSHL, New York, 1988).Methods of constructing such antibodies are discussed above, in Example10.

Any standard immunoassay format (for example, ELISA, Western blot, orRIA assay) can be used to measure BHD polypeptide or protein levelsand/or size; comparison is to wild-type (normal) BHD levels and/or size,and an alteration in BHD polypeptide may be indicative of an abnormalbiological condition such as BHD syndrome and/or a predilection todevelopment of spontaneous pneumothorax and/or renal neoplasia.Immunohistochemical techniques may also be utilized for BHD polypeptideor protein detection. For example, a tissue sample may be obtained froma subject, and a section stained for the presence of BHD using aBHD-specific binding agent (for example, anti-BHD antibody) and anystandard detection system (for example, one which includes a secondaryantibody conjugated to horseradish peroxidase). General guidanceregarding such techniques can be found in, for example, Bancroft andStevens (Theory and Practice of Histological Techniques, ChurchillLivingstone, 1982) and Ausubel et al (Current Protocols in MolecularBiology, John Wiley & Sons, New York 1998).

For the purposes of quantitating a BHD protein, a biological sample ofthe subject (which can be any animal, for instance a mouse or a human),which sample includes cellular proteins, is used. Such a biologicalsample may be obtained from body cells, such as those present inperipheral blood, urine, saliva, tissue biopsy, amniocentesis samples,surgical specimens and autopsy material, particularly breast cells.Quantitation of BHD protein can be achieved by immunoassay and comparedto levels of the protein found in control cells (for example, healthy,as in from a subject known not to have BHD syndrome or relatedsymptoms). A significant (for example, 10% or greater) reduction in theamount of BHD protein in the cells of a subject compared to the amountof BHD protein found in normal human cells could be taken as anindication that the subject may have deletions or mutations in the BHDgene, whereas a significant (for example, 10% or greater) increase wouldindicate that a duplication (amplification), or mutation that increasesthe stability of the BHD protein or mRNA, may have occurred. Deletion,mutation, and/or amplification of or within the BHD encoding sequence,and substantial under- or over-expression of BHD protein, is indicativeof BHD syndrome and/or a predilection to develop spontaneouspneumothorax and/or renal neoplasia.

Example 13 Differentiation of Individuals Homozygous Versus Heterozygousfor BHD Mutation(s)

As will be appreciated, the oligonucleotide ligation assay (OLA), asdescribed at Nickerson et al. (Proc. Natl. Acad. Sci. USA 87:8923-8927,1990), allows the differentiation between individuals who are homozygousversus heterozygous for specific BHD mutations, such as for instancethose mutations listed in Table 3. This feature allows one to rapidlyand easily determine whether an individual is homozygous for at leastone BHD mutation, which mutation is linked to BHD and/or a relativelyhigh predisposition to developing BHD syndrome and/or an increasedlikelihood of experiencing spontaneous pneumothorax and/or developingrenal neoplasia Alternatively, OLA can be used to determine whether asubject is homozygous for any of these mutations.

As an example of the OLA assay, when carried out in microtiter plates,one well is used for the determination of the presence of the BHD allelethat contains a C at nucleotide position 1844 and a second well is usedfor the determination of the presence of the BHD allele that contains aG at nucleotide position 1844. Thus, the results for an individual whois heterozygous for the C1844G mutation will show a signal in each ofthe C and G wells, and an individual who is homozygous for the mutantC1844G mutation will show a signal in only the G well. A skilledpractitioner will understand how to design other oligonucleotides forother OLA assays to be used in detecting the several mutations describedherein, as well as others identified based on the specific disclosedmutations.

Example 14 Suppression of BHD Protein Expression

A reduction of BHD protein expression in a transgenic cell may beobtained by introducing into cells an antisense construct based on theBHD encoding sequence, including the human BHD cDNA (Accession numberAF517523; SEQ ID NO: 1) or gene sequence or flanking regions thereof.For antisense suppression, a nucleotide sequence from a BHD encodingsequence, for example all or a portion of the BHD cDNA or gene, isarranged in reverse orientation relative to the promoter sequence in thetransformation vector. Other aspects of the vector may be chosen asdiscussed above (Example 9).

The introduced sequence need not be the full length human BHD cDNA orgene or reverse complement thereof, and need not be exactly homologousto the equivalent sequence found in the cell type to be transformed.Generally, however, where the introduced sequence is of shorter length,a higher degree of homology to the native BHD sequence will be neededfor effective antisense suppression. The introduced antisense sequencein the vector may be at least 30 nucleotides in length, and improvedantisense suppression will typically be observed as the length of theantisense sequence increases. The length of the antisense sequence inthe vector advantageously may be greater than 100 nucleotides. Forsuppression of the BHD gene itself, transcription of an antisenseconstruct results in the production of RNA molecules that are thereverse complement of mRNA molecules transcribed from the endogenous BHDgene in the cell.

Although the exact mechanism by which antisense RNA molecules interferewith gene expression has not been elucidated, it is believed thatantisense RNA molecules bind to the endogenous mRNA molecules andthereby inhibit translation of the endogenous mRNA.

Suppression of endogenous BHD expression can also be achieved usingribozymes. Ribozymes are synthetic RNA molecules that possess highlyspecific endoribonuclease activity. The production and use of ribozymesare disclosed in U.S. Pat. No. 4,987,071 to Cech and U.S. Pat. No.5,543,508 to Haselhoff. The inclusion of ribozyme sequences withinantisense RNAs may be used to confer RNA cleaving activity on theantisense RNA, such that endogenous mRNA molecules that bind to theantisense RNA are cleaved, which in turn leads to an enhanced antisenseinhibition of endogenous gene expression.

Suppression can also be achieved using RNA interference, using known andpreviously disclosed methods. Several models have been put forward toexplain RNAi, in particular the mechanisms by which the cleavage derivedsmall dsRNAs or siRNAs interact with the target mRNA and thus facilitateits degradation (Hamilton et al., Science 286, 950, 1999; Zamore et al.,Cell 101, 25, 2000; Hammond et al., Nature 404, 293, 2000; Yang et al.,Curr. Biol. 10, 1191, 2000; Elbashir et al., Genes Dev. 15, 188, 2001;Bass Cell 101, 235, 2000). It has been proposed that the cleavagederived small dsRNAs or siRNAs act as a guide for the enzymatic complexrequired for the sequence specific cleavage of the target mRNA. Evidencefor this includes cleavage of the target mRNA at regular intervals of˜21-23 nts in the region corresponding to the input dsRNA (Zamore et al,Cell 101, 25, 2000), with the exact cleavage sites corresponding to themiddle of sequences covered by individual 21- or 22 nt small dsRNAS orsiRNAs (Elbashir et al., Genes Dev. 15, 188, 2001). Although mammals andlower organisms appear to share dsRNA-triggered responses that involve arelated intermediate (small dsRNAs), it is likely that there will bedifferences as well as similarities in the underlying mechanism. dsRNAscan be formed from RNA oligomers produced synthetically (for technicaldetails see material from the companies Xeragon and Dharmacon, bothavailable on the internet). Small dsRNAs and siRNAs can also bemanufactured using standard methods of in vitro RNA production. Inaddition, the Silencer™ siRNA Construction kit (and components thereof)available from Ambion (Catalog # 1620; Austin, Tex.), which employs a T7promoter and other well known genetic engineering techniques to producedsRNAs. Double stranded RNA triggers could also be expressed from DNAbased vector systems.

Finally, dominant negative mutant forms of BHD may be used to blockendogenous BHD activity.

Example 15 BHD Gene Therapy

Gene therapy approaches for combating BHD syndrome and associatedsymptoms, or reducing the risk of developing spontaneous pneumothoraxand/or renal neoplasia, in subjects are now made possible by the presentdisclosure.

Retroviruses have been considered a preferred vector for experiments ingene therapy, with a high efficiency of infection and stable integrationand expression (Orkin et al., Prog. Med. Genet. 7:130-142, 1988). Thefull-length BHD gene or cDNA can be cloned into a retroviral vector anddriven from either its endogenous promoter or from the retroviral LTR(long terminal repeat). Other viral transfection systems may also beutilized for this type of approach, including adenovirus,adeno-associated virus (AAV) (McLaughlin et al., J. Virol. 62:1963-1973,1988), Vaccinia virus (Moss et al., Annu. Rev. Immunol. 5:305-324,1987), Bovine Papilloma virus (Rasmussen et al., Methods Enzymol.139:642-654, 1987) or members of the herpesvirus group such asEpstein-Barr virus (Margolskee et al., Mol. Cell. Biol. 8:2837-2847,1988).

Recent developments in gene therapy techniques include the use ofRNA-DNA hybrid oligonucleotides, as described by Cole-Strauss, et al.(Science 273:1386-1389, 1996). This technique may allow forsite-specific integration of cloned sequences, thereby permittingaccurately targeted gene replacement.

In addition to delivery of a BHD-encoding sequence to cells using viralvectors, it is possible to use non-infectious methods of delivery. Forinstance, lipidic and liposome-mediated gene delivery has recently beenused successfully for transfection with various genes (for reviews, seeTempleton and Lasic, Mol. Biotechnol. 11:175-180, 1999; Lee and Huang,Crit. Rev. Ther. Drug Carrier Syst. 14:173-206; and Cooper, Semin.Oncol. 23:172-187, 1996). For instance, cationic liposomes have beenanalyzed for their ability to transfect monocytic leukemia cells, andshown to be a viable alternative to using viral vectors (de Lima et al.,Mol. Membr. Biol. 16:103-109, 1999). Such cationic liposomes can also betargeted to specific cells through the inclusion of, for instance,monoclonal antibodies or other appropriate targeting ligands (Kao etal., Cancer Gene Ther. 3:250-256, 1996).

To reduce the level of BHD expression, gene therapy can be carried outusing antisense or other suppressive constructs, the construction ofwhich is discussed above (Example 13).

Example 16 Incorporation of Folliculin Protein into PharmaceuticalCompositions

Pharmaceutical compositions that comprise at least one folliculinprotein or fragment thereof as an active ingredient will normally beformulated with an appropriate solid or liquid carrier, depending uponthe particular mode of administration chosen. The pharmaceuticallyacceptable carriers and excipients useful in this invention areconventional. For instance, parenteral formulations usually compriseinjectable fluids that are pharmaceutically and physiologicallyacceptable fluid vehicles such as water, physiological saline, otherbalanced salt solutions, aqueous dextrose, glycerol or the like.Excipients that can be included are, for instance, other proteins, suchas human serum albumin or plasma preparations. If desired, thepharmaceutical composition to be administered may also contain minoramounts of non-toxic auxiliary substances, such as wetting oremulsifying agents, preservatives, and pH buffering agents and the like,for example sodium acetate or sorbitan monolaurate.

The dosage form of the pharmaceutical composition will be determined bythe mode of administration chosen. For instance, in addition toinjectable fluids, topical and oral formulations can be employed.Topical preparations can include eye drops, ointments, sprays and thelike. Oral formulations may be liquid (for example, syrups, solutions orsuspensions), or solid (for example, powders, pills, tablets, orcapsules). For solid compositions, conventional non-toxic solid carrierscan include pharmaceutical grades of mannitol, lactose, starch, ormagnesium stearate. Actual methods of preparing such dosage forms areknown, or will be apparent, to those skilled in the art.

The pharmaceutical compositions that comprise folliculin protein willpreferably be formulated in unit dosage form, suitable for individualadministration of precise dosages. One possible unit dosage containsapproximately 100 μg of protein. The amount of active compoundadministered will be dependent on the subject being treated, theseverity of the affliction, and the manner of administration, and isbest left to the judgment of the prescribing clinician. Within thesebounds, the formulation to be administered will contain a quantity ofthe active component(s) in an amount effective to achieve the desiredeffect in the subject being treated.

Example 17 Kits

Kits are provided which contain the necessary reagents for determiningthe presence or absence of mutation(s) in a BHD-encoding sequence, suchas probes or primers specific for the BHD gene. Such kits can be usedwith the methods described herein to determine whether a subject ispredisposed to BHD syndrome and/or spontaneous pneumothorax and/or renalneoplasia.

The provided kits may also include written instructions. Theinstructions can provide calibration curves or charts to compare withthe determined (for example, experimentally measured) values. Kits arealso provided to determine elevated or depressed expression of mRNA (forexample, containing probes) or BHD protein (for example, containingantibodies or other folliculin specific binding agents).

A. Kits for Amplification of BHD Sequences

The nucleic acid molecules disclosed herein, and oligonucleotide probesand primers derived therefrom, can be supplied in the form of a kit foruse in detection of a predisposition to BHD syndrome or spontaneouspneumothorax and/or renal neoplasia in a subject. In such a kit, anappropriate amount of one or more of the oligonucleotide primers isprovided in one or more containers. Oligonucleotide primers may beprovided suspended in an aqueous solution or as a freeze-dried orlyophilized powder, for instance. The container(s) in which theoligonucleotide(s) are supplied can be any conventional container thatis capable of holding the supplied form, for instance, microfuge tubes,ampoules, or bottles. In some applications, pairs of primers may beprovided in pre-measured single use amounts in individual, typicallydisposable, tubes or equivalent containers. With such an arrangement,the sample to be tested for the presence of a BHD mutation can be addedto the individual tubes and amplification carried out directly.

The amount of each oligonucleotide primer supplied in the kit can be anyappropriate amount, depending for instance on the market to which theproduct is directed. For instance, if the kit is adapted for research orclinical use, the amount of each oligonucleotide primer provided wouldlikely be an amount sufficient to prime several PCR amplificationreactions. Those of ordinary skill in the art know the amount ofoligonucleotide primer that is appropriate for use in a singleamplification reaction. General guidelines may for instance be found inInnis et al. (PCR Protocols, A Guide to Methods and Applications,Academic Press, Inc., San Diego, Calif., 1990), Sambrook et al. (InMolecular Cloning: A Laboratory Manual, Cold Spring Harbor, N.Y., 1989),and Ausubel et al. (In Current Protocols in Molecular Biology, GreenePubl. Assoc. and Wiley-Intersciences, 1992).

A kit may include more than two primers, in order to facilitate the invitro amplification of BHD sequences, for instance the BHD gene or the5′ or 3′ flanking region thereof.

In some embodiments, kits may also include the reagents necessary tocarry out nucleotide amplification reactions, including, for instance,DNA sample preparation reagents, appropriate buffers for example,polymerase buffer), salts (for example, magnesium chloride), anddeoxyribonucleotides (dNTPs).

Kits may in addition include either labeled or unlabeled oligonucleotideprobes for use in detection of BHD mutation(s). In certain embodiments,these probes will be specific for a potential mutation that may bepresent in the target-amplified sequences. The appropriate sequences forsuch a probe will be any sequence that includes one or more of theidentified mutant sites, particularly nucleotide positions (numbered asin SEQ ID NO: 1 unless otherwise stated) 1087 and/or 1088, all or aportion of positions 1378-1405 (or 1378-1405 of SEQ ID NO: 5), 1733through 1741, and 1844, such that the sequence of the probe iscomplementary to a mutant site and the surrounding BHD sequence.

It may also be advantageous to provide in the kit one or more controlsequences for use in the amplification reactions. The design ofappropriate positive control sequences is well known to one of ordinaryskill in the appropriate art.

B. Kits for Detection of BHD mRNA Expression

Kits similar to those disclosed above for the detection of BHD mutationsdirectly can be used to detect BHD mRNA expression, such as over- orunder-expression. Such kits include an appropriate amount of one or moreoligonucleotide primers for use in, for instance, reverse transcriptionPCR reactions, similarly to those provided above with art-obviousmodifications for use with RNA amplification.

In some embodiments, kits for detection of altered expression of BHDmRNA may also include some or all of the reagents necessary to carry outRT-PCR in vitro amplification reactions, including, for instance, RNAsample preparation reagents (including, for example, an RNaseinhibitor), appropriate buffers (for example, polymerase buffer), salts(for example, magnesium chloride), and deoxyribonucleotides (dNTPs).Written instructions may also be included.

Such kits may in addition include either labeled or unlabeledoligonucleotide probes for use in detection of the in vitro amplifiedtarget sequences. The appropriate sequences for such a probe will be anysequence that falls between the annealing sites of the two providedoligonucleotide primers, such that the sequence the probe iscomplementary to is amplified during the PCR reaction. In certainembodiments, these probes will be specific for a potential mutation thatmay be present in the target amplified sequences, for instance specificfor the 1087delAGinsC allele (for example, capable of detecting a Cresidue at position 1087 of the BHD sequence instead of the AG that isfound in wildtype). Other embodiment kits include probes specific forthe 1378 through 1405 duplication mutation, the 1733insC and 1733delCframeshift mutations, and the C1844G premature termination mutation.

It may also be advantageous to provide in the kit one or more controlsequences for use in the RT-PCR reactions. The design of appropriatepositive control sequences is well known to one of ordinary skill in theappropriate art.

Alternatively, kits may be provided with the necessary reagents to carryout quantitative or semi-quantitative Northern analysis of BHD mRNA.Such kits include, for instance, at least one BHD-specificoligonucleotide for use as a probe. This oligonucleotide may be labeledin any conventional way, including with a selected radioactive isotope,enzyme substrate, co-factor, ligand, chemiluminescent or fluorescentagent, hapten, or enzyme. In certain embodiments, such probes will bespecific for a potential mutation that may be present in the targetamplified sequences, for instance specific for the 1087delAGinsC allele(for example, capable of detecting a C residue at position 1087 of theBHD sequence instead of the AG that is found in wildtype). Otherembodiment kits include probes specific for the 1378 through 1405duplication mutation, the 1733insC and 1733delC frameshift mutations,and the C1844G premature termination mutation.

C. Kits for Detection of BHD (Folliculin) Protein Expression

Kits for the detection of BHD protein expression (such as over- orunder-expression) are also encompassed. Such kits may include at leastone target protein specific binding agent (for example, a polyclonal ormonoclonal antibody or antibody fragment that specifically recognizesthe BHD protein, folliculin) and may include at least one control (suchas a determined amount of BHD protein, or a sample containing adetermined amount of BHD protein). The folliculin-protein specificbinding agent and control may be contained in separate containers.

BHD protein expression detection kits may also include a means fordetecting BHD:binding agent complexes, for instance the agent may bedetectably labeled. If the detectable agent is not labeled, it may bedetected by second antibodies or protein A for example, which may alsobe provided in some kits in one or more separate containers. Suchtechniques are well known.

Additional components in specific kits may include instructions forcarrying out the assay. Instructions will allow the tester to determinewhether BHD expression levels are elevated. Reaction vessels andauxiliary reagents such as chromogens, buffers, enzymes, etc. may alsobe included in the kits.

D. Kits for Detection of Homozygous versus Heterozygous Allelism

Also provided are kits that allow differentiation between individualswho are homozygous versus heterozygous for the 1087delAGinsC, 1378→1405dup, a 1733insC or 1733delC, or the C1844G mutations of BHD. Such kitsprovide the materials necessary to perform oligonucleotide ligationassays (OLA), as described by Nickerson et al. (Proc. Natl. Acad. Sci.USA 87:8923-8927, 1990) and herein. In specific embodiments, these kitscontain one or more microtiter plate assays, designed to detectmutation(s) in the BHD sequence of a subject, as described herein.

Additional components in some of these kits may include instructions forcarrying out the assay. Instructions will allow the tester to determinewhether a BHD allele is homozygous or heterozygous. Reaction vessels andauxiliary reagents such as chromogens, buffers, enzymes, etc. may alsobe included in the kits.

It may also be advantageous to provide in the kit one or more controlsequences for use in the OLA reactions. The design of appropriatepositive control sequences is well known to one of ordinary skill in theappropriate art.

Example 18 BHD Knockout and Overexpression Transgenic Animals

Mutant organisms that under-express or over-express the BHD proteinfolliculin are useful for research, for instance. Such mutants allowinsight into the physiological and/or pathological role of BHD in ahealthy and/or pathological organism. These mutants are “geneticallyengineered,” meaning that information in the form of nucleotides hasbeen transferred into the mutant's genome at a location, or in acombination, in which it would not normally exist. Nucleotidestransferred in this way are said to be “non-native.” For example, anon-BHD promoter inserted upstream of a native BHD-encoding sequencewould be non-native. An extra copy of a BHD gene on a plasmid,transformed into a cell, would be non-native.

Mutants may be, for example, produced from mammals, such as mice, thateither over-express folliculin or under-express folliculin, or that donot express folliculin at all. Over-expression mutants are made byincreasing the number of BHD genes in the organism, or by introducing aBHD gene into the organism under the control of a constitutive orinducible or viral promoter such as the mouse mammary tumor virus (MMTV)promoter or the whey acidic protein (WAP) promoter or themetallothionein promoter. Mutants that under-express folliculin may bemade by using an inducible or repressible promoter, or by deleting theBHD gene, or by destroying or limiting the function of the BHD gene, forinstance by disrupting the gene by transposon insertion.

Antisense genes may be engineered into the organism, under aconstitutive or inducible promoter, to decrease or prevent folliculinexpression, as discussed above in Example 11.

A gene is “functionally deleted” when genetic engineering has been usedto negate or reduce gene expression to negligible levels. When a mutantis referred to in this application as having the BHD gene altered orfunctionally deleted, this refers to the BHD gene and to any ortholog ofthis gene. When a mutant is referred to as having “more than the normalcopy number” of a gene, this means that it has more than the usualnumber of genes found in the wild-type organism, for example, in thediploid mouse or human.

A mutant mouse or other mammal over-expressing folliculin may be made byconstructing a plasmid having a BHD encoding sequence driven by apromoter, such as the mouse mammary tumor virus (MMTV) promoter or thewhey acidic protein (WAP) promoter. This plasmid may be introduced intomouse oocytes by microinjection. The oocytes are implanted intopseudopregnant females, and the litters are assayed for insertion of thetransgene. Multiple strains containing the transgene are then availablefor study.

WAP is quite specific for mammary gland expression during lactation, andMMTV is expressed in a variety of tissues including mammary gland,salivary gland, and lymphoid tissues. Many other promoters might be usedto achieve various patterns of expression, for example, themetallothionein promoter.

An inducible system may be created in which the subject expressionconstruct is driven by a promoter regulated by an agent that can be fedto the mouse, such as tetracycline. Such techniques are well known inthe art.

A mutant knockout animal (for example, mouse) from which a BHD gene isdeleted can be made by removing all or some of the coding regions of theBHD gene from embryonic stem cells. The methods of creating deletionmutations by using a targeting vector have been described (Thomas andCapecch, Cell 51:503-512, 1987).

A mutant knockout animal (for example mouse) can be made by conditionalBHD gene targeting using Cre/lox site-specific recombination technologyand deleting the BHD gene in a tissue-(for example, skin) ortime-dependent manner.

Example 19 Knock-in Organisms

In addition to knock-out systems, it is also beneficial to generate“knock-ins” that have lost expression of the wildtype protein but havegained expression of a different, usually mutant form of the sameprotein. By way of example, the mutant BHD proteins (folliculins)provided herein (for example, in SEQ ID NO: 4, 6, 8, 10, and 12) can beexpressed in a knockout background in order to provide model systems forstudying the effects of these mutants. In particular embodiments, theresultant knock-in organisms provide systems for studying neoplasia,such as renal neoplasia.

Those of ordinary skill in the relevant art know methods of producingknock-in organisms. See, for instance, Rane et al. (Germ linetransmission of the Cdk4(R24C) mutation facilitates tumorigenesis andescape from cellular senescence. Mol. Cell Biol., 22: 644-656, 2002);Sotillo et al. (Wide spectrum of tumors in knock-in mice carrying a Cdk4protein insensitive to INK4 inhibitors. EMBO J., 20: 6637-6647, 2001);Luo et al. (Knock-in mice with a chimeric human/murine p53 gene developnormally and show wild-type p53 responses to DNA damaging agents: a newbiomedical research tool. Oncogene, 20: 320-328, 2001); Tomasson et al.(TEL/PDGFbetaR induces hematologic malignancies in mice that respond toa specific tyrosine kinase inhibitor. Blood, 93: 1707-1714, 1999);Voncken et al. (BCR/ABL P210 and P190 cause distinct leukemia intransgenic mice. Blood, 86: 4603-4611, 1995); Andrae et al. (A 1.8 kbGFAP-promoter fragment is active in specific regions of the embryonicCNS. Mech. Dev., 107: 181-185, 2001); Reinertsen et al. (Temporal andspatial specificity of PDGF alpha receptor promoter in transgenic mice.Gene Expr., 6: 301-314, 1997); Huang et al. (expression of greenfluorescent protein in oligodendrocytes in a time- andlevel-controllable fashion with a tetracycline-regulated system. Mol.Med., 5: 129-137, 1999); Reichert et al. (Treatment of Bcr/Ab1-positiveacute lymphoblastic leukemia in P190 transgenic mice with the farnesyltransferase inhibitor SCH66336. Blood, 97: 1399-1403, 2001); andHuettner et al. (Reversibility of acute B-cell leukaemia induced byBCR-ABL1. Nat. Genet., 24: 57-60, 2000), by way of example.

Example 20 Detection of Folliculin-Interacting Proteins

With the provision herein of the folliculin protein, and its link to BIDsyndrome, methods of identifying proteins that interact with folliculinare now enabled. The identification and study of such proteins will helpto characterize native and mutant functions of the folliculin proteins,and thus will contribute significantly understanding the native biologyof the protein as well as its contribution to BHD syndrome andassociated conditions.

There are many systems for the identification of protein-proteininteractions, which systems will be known to those of ordinary skill inthe art. Merely by way of example, the yeast two hybrid system (Song andField, Nature 340(6230): 245-246, 1989) and later developed systems canbe used to identify proteins that interact with folliculin or fragmentsor domains thereof. For a review of applications of the yeast two hybridsystem, see Gietz et al., (“Identification of proteins that interactwith a protein of interest: Applications of the yeast two-hybridsystem.” Mol. Cell Biochem. 172: 67-79, 1997). Systems for identifyingprotein-protein interactions are also described in the following patentdocuments: U.S. Pat. No. 5,637,463 “Methods to detect protein-proteininteractions”; U.S. Pat. No. 5,925,523 “Interaction trap assay,reagents, and uses thereof”; U.S. Pat. No. 5,928,868 “Three hybridscreening assay”; U.S. Pat. No. 5,955,280 “Reverse two-hybrid system”;U.S. Pat. No. 5,965,368 “Reverse two-hybrid system”; U.S. Pat. No.6,200,759 “Interaction trap assay, reagents, and uses thereof”; and U.S.Pat. No. 6,342,345 “Detection of molecular interactions by reportersubunit complementation.”

Merely by way of example, the Hybrid Hunter™ yeast two-hybrid systemfrom Invitrogen (Carlsbad, Calif.) can be used to screen a human cDNAlibrary for folliculin-binding or interacting proteins. Bait plasmidsare generated by PCR cloning full-length BHD encoding sequence or aportion thereof in-frame with the DNA-binding domain of LexA from thepHybLex/Zeo. The prey plasmid library can be generated by cloning ahuman cDNA library downstream of the B42 activator domain in thepYESTrp2 vector.

Bait plasmid is transformed into a yeast strain, such as L40 [MATahis3Δ200 trpl-901 leu2-3112 ade2 LYS2::(41exAop-1HS3)URA3::(81exAop-lacZ) GAL4] (Invitrogen, Carlsbad, Calif.) using thePEG/Li-acetate (Gietz et al., Nucleic Acids Res. 20:1425, 1992) oranother standard method. The cDNA library is then transformed into thesecells. Transformants growing on his⁻ media are tested using aβ-galactosidase filter lift assay (Invitrogen, Carlsbad, Calif.).Putative positive clones are indicated by blue colonies after 25 minutesin the 30° C. incubator. Putative positive clones are selected forfurther testing. Plasmid DNA extracted from the clones can betransformed into E. coli XL10-gold cells (Stratagene, La Jolla, Calif.),and then subjected to restriction analysis and/or sequence analysis.Each putative interactor can be checked for autoactivation and histidineprototrophy. Additional analysis using standard techniques can beperformed to test for and eliminate false positives.

In addition to the Hybrid Hunter™ system, commercial two-hybrid systemsare also available from other sources, including the Matchmaker™ LexAsystem from Clontech, the DupLEX-A ™ system from OriGene Technologies,Inc., and the DisplayGREEN Two-Hybrid Kit from Display System fromDisplay Systems Biotech.

Another method of identification of folliculin binding proteins is byGST-folliculin pull down assays (Kaelin et al., Cell 70:351, 1992).Another method is the use of peptide phage display technology (Sche etal., Chemistry & Biology 6:707, 1999).

This disclosure provides a new nucleic acid molecule, BHD, and theprotein encoded thereby (folliculin), along with several specific mutantBHD sequences and folliculin proteins that are linked to BHD syndrome,and more particularly to predisposition to or the condition ofspontaneous pneumothorax and/or renal neoplasia. The disclosure furtherprovides methods for identifying these mutations or mutant proteins in asubject, and using them to determine or predict a subject's BHD diseasestate. It will be apparent that the precise details of the methodsdescribed may be varied or modified without departing from the spirit ofthe described disclosure. We claim all such modifications and variationsthat fall within the scope and spirit of the claims below.

1. An isolated nucleic acid molecule comprising the sequence set forthin SEQ ID NO: 1, SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9,or SEQ ID NO:
 11. 2. A recombinant nucleic acid molecule comprising apromoter sequence operably linked to a nucleic acid molecule accordingto claim
 1. 3. An isolated cell transformed with a recombinant nucleicacid molecule according to claim
 1. 4. The cell of claim 3, wherein thecell is a non-human cell.
 5. A method of detecting a biologicalcondition associated with a mutant BHD nucleic acid in a subject,comprising determining whether the subject has mutant BHD nucleic acid,and wherein the mutant BHD nucleic acid comprises SEQ ID NO: 3, SEQ IDNO: 5, SEQ ID NO: 7, SEQ ID NO: 9, or SEQ ID NO:
 11. 6. The method ofclaim 5, wherein the mutant BHD nucleic acid encodes a truncatedfolliculin protein and the method comprises detecting the truncatedfolliculin protein.
 7. The method of claim 6, wherein the truncatedfolliculin protein comprises a sequence as set forth in SEQ ID NO: 4,SEQ ID NO: 6, SEQ ID NO: 8, SEQ ID NO: 10, or SEQ ID NO:
 12. 8. Themethod of claim 5, which is a method of detecting BHD syndrome.
 9. Themethod of claim 5, which is a method of detecting BHD-associatedspontaneous pneumothorax.
 10. The method of claim 5, which is a methodof detecting BHD-associated renal neoplasia.
 11. A method comprising: a.obtaining a sample of nucleic acid from a subject; and b. determiningthe presence of nucleotides that result in truncation of a BHD protein,wherein the truncated BHD protein is encoded by a nucleic acid moleculethat comprises SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 7,SEQ ID NO: 9, orSEQ ID NO:
 11. 12. The method of claim 11, wherein the determining stepcomprises amplifying at least that portion of the nucleic acid moleculeencoding the truncated BHD protein which includes the nucleotides thatresult in the truncation.
 13. The method of claim 11, wherein thedetermining step comprises sequencing at least that portion of thenucleic acid molecule encoding the truncated BHD protein which includesthe nucleotides that result in the truncation.
 14. The method of claim11, wherein the method comprises determining a propensity to develop acondition associated with BHD disease.
 15. The method of claim 14,wherein the condition comprises fibrofolliculoma, renal neoplasia, orspontaneous pneumothorax.
 16. The method of claim
 5. wherein the subjecthas a mutated BHD nucleic acid and wherein detecting comprises detectinga mutation within nucleotides 1733-1740 of SEQ ID NO:
 1. 17. The methodof claim 5, wherein detecting comprises detecting one or more of themutations listed in Table
 2. 18. A transgenic non-human animaltransformed with a recombinant nucleic acid molecule according to claim1.